Erzeugung von N,N-disubstituierten Iminiumsalzen mit Hilfe von Silan-Reagenzien

Generation of N,N-Disubstituted Iminium Salts by Application of Silane Reagents (Dialkylamino)trimethylsilanes, halotrimethylsilanes and trimethylsilyl triflate proved to be superior reagents for a convenient access to the title compounds in an aprotic medium. In most cases, the co-formation of silylethers or disiloxanes acts as driving force. A comprehensive overview on this field, including the latest findings, is given and the significant mechanistic relationships are illuminated. The three component synthesis starting from carbonyl compounds (Scheme 3) and the two component synthesis (“latent” three component synthesis) starting from α-chloroethers (Schemes 16, 19) hold a central position. The latter method offers special advantage for the entrance into the multifunctional series, as shown by the first synthesis of vinylogous Viehe salts as preparatively useful C₃-building blocks (Schemes 17, 22, 23). As an aim, this report should stimulate further progress in these areas.     

Asymmetric Aza‐Morita–Baylis–Hillman‐Type Reactions: The Highly Enantioselective Reaction between Unmodified α,β‐ Unsaturated Aldehydes and N‐Acylimines by Organo‐co‐catalysis

The highly enantioselective organo‐co‐catalytic aza‐Morita–Baylis–Hillman (MBH)‐type reaction between N‐carbamate‐protected imines and α,β‐unsaturated aldehydes has been developed. The organic co‐catalytic system of proline and 1,4‐diazabicyclo[2.2.2]octane (DABCO) enables the asymmetric synthesis of the corresponding N‐Boc‐ and N‐Cbz‐protected β‐amino‐α‐alkylidene‐aldehydes in good to high yields and up to 99% ee. In the case of aza‐MBH‐type addition of enals to phenylprop‐2‐ene‐1‐imines, the co‐catalytic reaction exhibits excellent 1,2‐selectivity. The organo‐co‐catalytic aza‐MBH‐type reaction can also be performed by the direct highly enantioselective addition of α,β‐unsaturated aldehydes to bench‐stable N‐carbamate‐protected α‐amidosulfones to give the corresponding β‐amino‐α‐alkylidene‐aldehydes with up to 99% ee. The organo‐co‐catalytic aza‐MBH‐type reaction is also an expeditious entry to nearly enantiomerically pure β‐amino‐α‐alkylidene‐amino acids and β‐amino‐α‐alkylidene‐lactams (99% ee). The mechanism and stereochemistry of the chiral amine and DABCO co‐catalyzed aza‐MBH‐type reaction are also discussed.     

Eine neue,breit anwendbare Synthese für aromatische Aldehyde

Diformamide ( 1 ) reacts with activated aromatic compounds like toluene, anisole, m‐xylene, 1,2‐dimethoxybenzene in the presence of AlCl₃ to give N‐(diarylmethyl)‐formamides 2a—d , the corresponding aromatic aldehydes 3—6 are formed as by‐products in low yields. From N,N‐dimethylaniline and 1 /AlCl₃ the triphenylmethane derivative 7 can be obtained. The reaction of anisole with N‐methyl‐diformamide ( 9 ) affords the formamide 10 . The mixture of formamide, P₄O₁₀ and AlCl₃ reveals to be a reagent which is capable to formylate toluene and anisole, resp. Triformamide ( 14 )/AlCl₃ is an effective formylating system which allows the preparation of aromatic aldehydes (e.g. 3,4,17—32 ) from the corresponding aromatic hydrocarbons. Aluminiumchloride can be replaced by borontrichloride. The yields of the formylation reactions depend strongly from the reaction conditions (molar ratio: aromatic hydrocarbon/AlCl₃/ 14 ; solvent, reaction temperature). The scope of the reaction covers nearly complete those of the Gattermann‐Koch‐, Gattermann‐ and Vilsmeier—Haack‐reaction.     

Chiral Thiourea‐Phosphine Organocatalysts in the Asymmetric Aza‐Morita–Baylis–Hillman Reaction

A new kind of bifunctional (thio)urea‐phosphine catalyst was synthesized and applied to the aza‐Morita–Baylis–Hillman reaction of N‐sulfonated imines with methyl vinyl ketone, phenyl vinyl ketone, ethyl vinyl ketone or acrolein. Moderate to excellent ee and yields of the products were obtained under mild reaction conditions.     

Industrielle Bedeutung der Vilsmeier–Haack-Reaktion in der Farbstoffchemie

Vilsmeier–Haack Formylation Reaction – Importance in Colour Industry The Vilsmeier-Haack reaction which has been discovered in 1927 is being used in industry to formylate alkylated aromatic amines and related compounds. Roughly 2000 tons of formylation products are yearly produced in the world. Preferably they are used as building blocks in dye chemistry. Many classes of dyes like cyanines, coumarin dyes, merocyanines, cationic dyes, color formers or dyes for non linear optical applications are being obtained from „Vilsmeier”︁ products. Different conditions of the Vilsmeier-Haack reaction and alternative routes for the introduction of a formyl group are discussed in this progress report.     

Tunable Bifunctional Phosphine–Squaramide Promoted Morita–Baylis–Hillman Reaction of N‐Alkyl Isatins with Acrylates

A series of highly tunable bifunctional phosphine‐squaramide H‐bond donor organocatalysts 6 has been synthesized from inexpensive and commercially available β‐amino alcohols in moderate yields. Catalyst 6 f can efficiently promote the asymmetric Morita–Baylis–Hillman (MBH) reaction of N‐alkyl isatins with acrylate esters providing the chiral 3‐substituted 3‐hydroxy‐2‐oxindoles in good yields and enantioselectivities (up to 93 % yield and 95 % ee), in which the challenging substrate tert‐butyl acrylate 9 d , provided the best ee value to date. Moreover, this methodology was applied successfully in the synthesis of chiral cyclic spiropyrrolizidineoxindole and γ‐butyrolactone derivatives without enantioselectivity deterioration. The possible mechanism of this MBH reaction was also investigated by ³¹P NMR, ESI‐MS and KIE studies. The KIE experiments show that the electrophilic addition of N‐methyl isatin to the complex of acrylate ester and phophine‐squaramide is the rate‐determing step of the asymmetric MBH reaction.

     

Stereoselective Cascade Reactions of Donor–Acceptor Cyclopropanes with m‐N,N‐Dialkylaminophenyl α,β‐Unsaturated Carbonyls: Diastereoselective Synthesis of cis‐ and trans‐Tetralins

The ytterbium(III) triflate [Yb(OTf)₃]‐catalyzed diastereoselective cascade reaction of m‐N,N‐dimethylaminophenyl α,β‐unsaturated carbonyls with cyclopropane 1,1‐diesters under mild reaction conditions afforded highly substituted cis‐ and trans‐tetralins. The reaction of m‐N,N‐dimethylaminophenyl α,β‐unsaturated ketones with cyclopropane 1,1‐diesters provided tetralins with a trans orientation of the 1,4‐substitutents on the cyclohexyl ring; cis‐tetralins were obtained from m‐N,N‐dimethylaminophenyl substituted methylidenemalonates with high diastereoselectivities.

     

Dendritic Chiral Phosphine Lewis Bases‐Catalyzed Asymmetric Aza‐Morita–Baylis–Hillman Reaction of N‐Sulfonated Imines with Activated Olefins

A series of polyether dendritic chiral phosphine Lewis bases was synthesized, and successfully applied to the asymmetric aza‐Morita–Baylis–Hillman reaction of N‐sulfonated imines (N‐arylmethylidene‐4‐methylbenzenesulfonamides) with methyl vinyl ketone (MVK), ethyl vinyl ketone (EVK), and acrolein to give the adducts in good to excellent yields along with up to 97 % ee, which are more effective than our previously reported original chiral phosphine Lewis bases. In addition, the dendrimer‐supported chiral phosphine Lewis bases can be easily recovered and reused.     

N,N‐dichloro poly(styrene‐co‐divinyl benzene) sulfonamide polymeric beads: An efficient and recyclable decontaminating reagent for O,S‐diethyl methyl phosphonothiolate,a simulant of VX

An efficient and operationally simple method is developed for chemical decontamination of simulant of VX. A new chlorine bearing reagent N,N‐dichloro poly(styrene‐co‐divinyl benzene) sulfonamide was developed to deactivate the simulant of VX in aqueous medium. This decontamination reaction was monitored by gas chromatography (GC), and the products were analyzed by gas chromatography‐mass spectrometry (GC‐MS). This reagent has advantage over earlier reported reagents in terms of effectiveness, stability, nontoxicity, cost, ease of synthesis, recyclablity (collected after filtration, rechlorinated, and used for further reaction), and decontamination of simulant of VX to give single nontoxic product at room temperature. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Friedel–craft N-alkylation and N-acylation of acrylamide: A novel approach for synthesis of alkylacrylamides

N-Alkylacrylamides and N-acylacrylamides were synthesized by a novel synthetic approach, namely, the Friedel–Craft reaction of acrylamide with alkyl chloride and acyl chloride, respectively. The reactions took place smoothly at room temperature and the time required for the reactions was very short. The monomers so synthesized were characterized by elemental analyses, IR, and ¹H-NMR spectroscopy. Characterization data are in agreement with the proposed structures of the products. Thus, a convenient method for the synthesis of N-alkylacrylamides was developed. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 1845–1850, 1999     

Modification of Acid Anhydride-cured Epoxy Resins By N-Phenyl- maleimide–Styrene Copolymers and N-Phenylmaleimide–Styrene– p-Hydroxystyrene Terpolymers

N-Phenylmaleimide–styrene copolymers (PMS) and reactive N-phenylmaleimide–styrene–p-hydroxystyrene (HSt) terpolymers (PMSH) containing p-hydroxyphenyl groups were used to improve the toughness of bisphenol A diglycidyl ether epoxy resin cured with methyl hexahydrophthalic anhydride. PMS and PMSH were effective modifiers for epoxies. The morphologies of the modified resins depended on modifier structure and content. The most effective modification for the cured resins was attained because of the co-continuous structure of the modified resins in both PMS and PMSH modification systems. When using 15wt% of PMS (M¯_w 125000), the fracture toughness, K_IC, for the modified resin increased by 230%, with retention of flexural modulus and glass transition temperature, but with a loss of flexural strength, compared with the values for the unmodified epoxy resin. When using PMSH as the reactive modifier, the efficiency decreased with increase in HSt content, because of the increasing extent of dispersion of the PMSH-rich continuous phases. In the modification with 10wt% PMSH (1·0mol% HSt unit, M¯_w 294000), the modified resin had balanced physical properties. © of SCI.     

Aqueous and Solvent‐Free Uncatalyzed Three‐Component Vinylogous Mukaiyama–Mannich Reactions of Pyrrole‐Based Silyl Dienolates

A catalyst‐free, environmentally benign three‐component vinylogous Mukaiyama–Mannich reaction of pyrrole‐based silyl dienolates is presented, which works effectively in both aqueous and solvent‐free environments. Both lipophilic and hydrophilic aldehyde candidates are suitable substrates, allowing access to a rich repertoire of unsaturated vicinal aminolactam structures with virtually complete γ‐site selectivity and moderate to good anti‐diastereoselectivity. The utility of this technology is highlighted by protecting group‐free synthesis of densely hydroxylated, sugar‐related lactam frameworks. The role of water as an indispensable H‐bonding reaction propeller is demonstrated.     

Preparation and properties of a siloxane‐containing 2‐vinylpyridine–styrene–butadiene copolymer with water glass

A siloxane‐containing 2‐vinylpyridine–styrene–butadiene copolymer (PSBR/WG) was prepared from a 2‐vinylpyridine–styrene–butadiene copolymer (PSBR) latex and water glass. The water glass was added slowly, with stirring, to the PSBR latex. The latex mixture was stirred for 3 h at room temperature, and then, it was coagulated with 1N sulfuric acid producing a sulfate of PSBR with siloxane. The physical properties, such as the filling and stiffening effects of the hybrid polymer, and the vulcanizates were improved. An important advantage of this system is that it is possible to prepare the hybrid polymer simply, and the sodium ions formed in the reaction can also be easily removed. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 891–899, 2006     

Efficient Synthesis of 9‐Tosylaminofluorene Derivatives by Boron Trifluoride Etherate‐Catalyzed Aza‐Friedel–Crafts Reaction of in situ Generated N‐Tosylbenzaldimines

An efficient and expeditious boron trifluoride etherate (BF₃⋅Et₂O) catalyzed one‐pot reaction for the synthesis of N‐tosyl‐9‐aminofluorenes and anthracene derivatives from in situ generated N‐tosylbenzaldimines via an aza‐Friedal–Crafts reaction has been developed. The catalytic reaction shows high substrate tolerance with excellent yields.     

The polycondensation of lithium 11–bromoundecanoate in aqueous media

To obtain a biodegradable plastic, polycondensation, the substitution of bromine by carboxylate was carried out on lithium 11–bromoundecanoate. Using water as a solvent, the formation of a double bond was detected between 70 and 100°C, yielding a good quantity of polymer. Water is recommended as the best solvent for the reaction. Thermodynamic investigations were carried out by using ethylene glycol and water. The reaction is believed to proceed according to the S_N2 mechanism. The ΔH and ΔG values for condensation in ethylene glycol were slightly higher than for those in water, but the reaction rate in water at 70°C was 7 times greater than that in ethylene glycol. The enhancement of dissociation accounts for the advantageous condensation in aqueous media. Furthermore, ΔS shows negative values and ΔG shows positive values, meaning that the reaction should proceed exothermically and not spontaneously. Experiments to condense 11–bromoundecanoate in aqueous media were carried out for ten days in a water bath, kept at 70°C, using 25 mL of 0.05M 11–bromoundecanoate. The degree of polymerization for the resulting polymer was found to be 23 by the end group assay for both bromine and carboxylate. Neither a melting point nor glass transition point for the product were observed. The polymer formed decomposes at 300°C and instantly disperses. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 130–134, 2003     

Access to Stereodefined Trisubstituted Alkenes via Rhodium‐Catalyzed 1,4‐Addition of Potassium Trifluoro(organo)‐ borates to Baylis–Hillman Adducts

In the presence of a rhodium catalyst, unactivated Baylis–Hillman adducts reacted regioselectively with potassium trifluoro(organo)borates to afford stereodefined trisubstituted alkenes with good yields. This highly efficient reaction (aerobic conditions, low temperature, absence of added phosphane ligand) is believed to proceed via a 1,4‐addition/β‐hydroxy elimination mechanism.     

Enantioselective Aza‐Morita–Baylis–Hillman Reaction Using Aliphatic α‐Amidosulfones as Imine Surrogates

The bifunctional catalyst 6′‐deoxy‐6′‐acylamino‐β‐isocupreidine ( 1 ) served both as a base to trigger the in situ generation of N‐sulfonylimine from readily available α‐amidosulfones and as a chiral nucleophile to initiate the enantioselective aza‐Morita–Baylis–Hillman (aza‐MBH) reaction. α‐Methylene‐β‐amino‐β‐alkyl carbonyl compounds, difficultly accessible previously, can now be synthesized in excellent yields and enantioselectivities.     

Effect of a methyl substituent in the polymerization–crosslinking treatment of cotton with NMMA and NMA

An estimation of structures of reagent residues in cotton fabrics treated with N-methylolmethacrylamide (NMMA) and N-methylolacrylamide (NMA) and comparison of textile performance of the NMMA–cotton and NMA–cotton provide the basis for insight into the structure–performance relationship in these fabrics. The α-methyl substituent, which constitutes the difference between NMMA and NMA, accounts for an altered composition of reagent residues in the treated cotton. The more attractive balance of strength–abrasion resistance with resilience for the NMMA–cotton seems to be a result of a lower degree of covalent crosslinking, which appears compensated by a higher elastic modulus in the NMMA network polymer.     

Optimization of NOM Removal during Water Treatment

Abstract

The aim of this paper is to describe the removal efficiency of individual fractions of natural organic matter (NOM) and the aluminum transformation during treatment of two types of surface water with an increased concentration of NOM of various origins. The coagulation conditions (dose of destabilization reagent and reaction pH value) were optimized for the best NOM and aluminum removal. The results show that the NOM removal efficiency depends on the NOM character, using destabilizing reagents and reaction conditions. The optimized doses of destabilization reagents influence especially the removal of hydrophilic charged (CHA) and very hydrophobic acids (VHA) fractions during treatment of both types of raw water. In contrast to this, the removal of hydrophilic neutral (NEU) fraction is very low (? _NEU =0.13–0.22). The optimal destabilization reagent dosage is characterized by the lowest content of the total reactive aluminum concentration and relatively low concentration of dissolved organic aluminum.     

Iron‐Catalyzed Regio‐ and Stereoselective Conjugate Addition of Aryl‐Grignard Reagents to α,β,γ,δ‐Unsaturated Sulfones and its Synthetic Application

The iron‐catalyzed δ‐addition of aryl‐Grignard reagents to α,β,γ,δ‐unsaturated sulfones proceeded in a regio‐ and stereoselective manner to give cis‐4‐aryl‐2‐alkenyl sulfones. Allylic alkylation of the resultant products was performed without isomerization of the cis‐olefin to give cis‐4‐aryl‐1,1‐dialkyl‐2‐alkenyl sulfones, which upon intramolecular Friedel–Crafts reaction with aluminum chloride gave 1,4‐dihydronaphthalenes having a quaternary carbon center.