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1-氟-二苯[a,d]环庚酮的合成
引用本文:李雯,闫学斌,朱成功. 1-氟-二苯[a,d]环庚酮的合成[J]. 化学试剂, 2006, 28(7): 443-443,445
作者姓名:李雯  闫学斌  朱成功
作者单位:郑州大学,化工学院,河南,郑州,450002;郑州大学,新药研究中心,河南,郑州,450052;河南辅仁集团,河南,郑州,450008
摘    要:
以邻苯二甲酸酐和邻氟苯乙酸为原料,经高温缩合、还原、环化得到1-氟二苯[a,d]环庚酮,总收率为33.2%。该方法操作较简便,收率较高,具有工业生产价值。

关 键 词:1-氟-二苯[a  d]环庚酮  缩合  还原  环化  合成
文章编号:0258-3283(2006)07-0443-01
收稿时间:2005-12-04
修稿时间:2005-12-04

The synthesis of 1-fluoro-dibenzo [ a, d] cycloheptanone
LI Wen,YAN Xue-bin,ZHU Cheng-gong. The synthesis of 1-fluoro-dibenzo [ a, d] cycloheptanone[J]. Chemical Reagents, 2006, 28(7): 443-443,445
Authors:LI Wen  YAN Xue-bin  ZHU Cheng-gong
Affiliation:1. College of Chemical Engineering, Zhengzhou University, Zhengzhou 450002, China; 2. Research Center of New Drug, Zhengzhou University, Zhengzhou 450052, China; 3. Henan Furen Group, Zhengzhou 450008, China
Abstract:
1-Fluoro-dibenzo[a,d]cycloheptanone was synthesized from phthalic anhydride and orthofluorophenyl acetic acid as raw material by condensation under high temperature,reduction and cyclization.The total yield reached 33.2%.The method has high industrial value for its simplicity and high yield.
Keywords:1-fluoro-dibenzo[a  d]cycloheptanone  condensation  reduction  cyclization
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