详细信息
Preparation of 3-(4-chlorobutyl)-1H-indole-5-carbonitrile involves reacting sulfate group-containing compound with 1-chloro-4-bromo or iodobutane, and hydrolyzing butyl chloride compound in presence of alkali medium
文献类型:专利
英文题名:Preparation of 3-(4-chlorobutyl)-1H-indole-5-carbonitrile involves reacting sulfate group-containing compound with 1-chloro-4-bromo or iodobutane, and hydrolyzing butyl chloride compound in presence of alkali medium
作者:GUO J;HUANG R;SHEN Y;SHI J;TAO J;WANG C;ZHOU C
机构:[1]UNIV EAST CHINA SCI & TECHNOLOGY;[2]NANTONG HENGSHENG FINE CHEM CO LTD
申请号:CN103709089-B
公开日:2015-08-19
语种:英文
收录:DERWENT
摘要:NOVELTY - 5-Cyano indole ring and sulfonic acid compound (II) are reacted, to obtain sulfate group-containing compound (III). The sulfate group-containing compound (III) is reacted with 1-chloro-4-bromo or iodobutane to obtain butyl chloride compound (IV). The butyl chloride compound (IV) is hydrolyzed in presence of alkali medium, to obtain 3-(4-chlorobutyl)-1H-indole-5-carbonitrile (I). USE - Preparation of 3-(4-chlorobutyl)-1H-indole-5-carbonitrile (claimed). ADVANTAGE - The method provides 3-(4-chlorobutyl)-1H-indole-5-carbonitrile having high reaction selectivity without using expensive catalyst, with yield of 75.3%, by a controllable process. DETAILED DESCRIPTION - 5-Cyano indole ring and sulfonic acid compound of formula (II) are reacted, to obtain sulfate group-containing compound of formula (III). The sulfate group-containing compound (III) is reacted with 1-chloro-4-bromo or iodobutane to obtain butyl chloride compound of formula (IV). The butyl chloride compound (IV) is hydrolyzed in presence of alkali medium, to obtain 3-(4-chlorobutyl)-1H-indole-5-carbonitrile of formula (I). R=nitro or cyano;and X=Cl, or Br.
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