戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 263063作成日:2026年10月27日

Hydrochloric Acid → 3-Phenylindole-2-carbonitrile

https://huagongshe.com/reaction/263063

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物AnilineHCID 6115—
反応物Potassium HydroxideHCID 14797—
反応物Ethyl 2-cyano-3-phenylpropanoateHCID 228103—
反応物Sodium NitriteHCID 23668193—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物3-Phenylindole-2-carbonitrileHCID 12412080—

反応手順

A solution of 4.08 g. (0.044 mol) of aniline in 18 ml. of concentrated hydrochloric acid and 50 ml. of water was maintained below 5° while a solution of 3.00 g. (0.043 mol) of sodium nitrite in 10 ml. of water was added. This solution was then added to a mixture of 8.30 g. (0.041 mol) of α-cyanobenzenepropanoic acid ethyl ester, 50 ml. of ethanol, 100 ml. of water, and 18 ml. of 50% potassium hydroxide solution maintained below 0°. After stirring for an additional 20 minutes the reaction was diluted with water and shaken with ether. Some insoluble solid was removed by filtration and the ether layer was concentrated. The residue was heated on the steam bath for 4 hours with 60 ml. of acetic acid and 60 ml. of concentrated hydrochloric acid. The cooled reaction was diluted with water and extracted with dichloromethane. The extracts were dried, filtered over some silica gel and concentrated. Recrystallization of the residue from dichloromethane-hexane gave 3-phenylindole-2-carbonitrile as tan crystals, m.p. 137°-142°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04156016
出典データセットuspto-grants-1979_05
ORD IDord-59cd4715d355409f9aa5e6d3b8845c03
出典メモuspto-grants-1979_05