戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 414084作成日:2026年10月26日

Triphenylphosphine → 1-(Azidomethyl)-2-(trifluoromethyl)benzene

https://huagongshe.com/reaction/414084

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Hydrazoic acidHCID 24530—
反応物2-(Trifluoromethyl)benzylic alcoholHCID 67666—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
溶媒TolueneHCID 1140—
生成物1-(Azidomethyl)-2-(trifluoromethyl)benzeneHCID 16111739—

反応手順

First a solution of 17.4 g (0.1 mol) of azodicarboxylic acid diethyl ester in 50 ml of toluene is added dropwise at 10°-20° to a solution of 26.2 g (0.1 mol) of triphenylphosphine in 260 ml of toluene and then, at 5°-10°, a solution of 17.6 g (0.1 mol) of o-trifluoromethylbenzyl alcohol in 120 ml of a 1N solution of hydrazoic acid in toluene is added dropwise thereto and the whole is stirred at room temperature for 2 hours. The precipitated hydrazinodicarboxylic acid ester is filtered off with suction, the toluene solution is concentrated by evaporation and the residue is treated with cyclohexane. The cyclohexane solution is decanted off from the insoluble portions, filtered through a small amount of silica gel and concentrated by evaporation at 50° in vacuo. In this manner o-trifluoromethylbenzyl azide is obtained in the form of a colourless liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04789680
出典データセットuspto-grants-1988_12
ORD IDord-156194c0bb8242678777fa347e578fae
出典メモuspto-grants-1988_12