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9-蒽甲胺的合成
引用本文:王奇观,曹永军,王素敏. 9-蒽甲胺的合成[J]. 精细化工中间体, 2010, 40(2): 61-63
作者姓名:王奇观  曹永军  王素敏
作者单位:1. 西安工业大学,材料与化工学院,陕西,西安,710032
2. 驻马店教育学院,河南,驻马店,463000
摘    要:以9-蒽甲醇为原料,通过溴化、叠氮基亲核取代、催化氢化3步反应制备了9-蒽甲胺,总收率达60%。利用1HNMR、质谱、元素分析对产物的组成和结构进行了确认和鉴定。研究结果表明,以Pd/C为催化剂,催化氢化在常温常压下能够快速进行,40min就可完全反应。

关 键 词:9-蒽甲胺  9-蒽甲醇  合成

The Synthesis of 9-Aminomethylanthracene
WANG Qi-guan,CAO Yong-jun,WANG Su-min. The Synthesis of 9-Aminomethylanthracene[J]. Fine Chemical Intermediates, 2010, 40(2): 61-63
Authors:WANG Qi-guan  CAO Yong-jun  WANG Su-min
Affiliation:1. School of Material and Chemical Engineering, Xi'an Technological University, Xi'an 710032, China; 2. Zhumadian Institute of Education, Zhumadian 463000, China)
Abstract:9-Aminomethylanthracene is a versatile intermediate in organic synthesis. In this paper it was prepared from 9-anthylmethanol in three steps, including bromination, nucleophilic replacement with azid and Pd/C catalyzed hydrogenation, in 60% overall yield. The hydrogenation finished within 40 min at room temperature and under atmospheric pressure. The structure of the target compound was characterized with ^1H NMR, ESI-MS and elemental analysis.
Keywords:9-aminomethylanthracene  9-anthylmethanol  systhesis
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