戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 660822作成日:2026年10月26日

tert-Butanol → 2-benzyloxy-4-chloro-N-tert-butoxycarbonylaniline

https://huagongshe.com/reaction/660822

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物TriethylamineHCID 8471—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物2-(Benzyloxy)-4-chlorobenzoic acidHCID 22452154—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物2-benzyloxy-4-chloro-N-tert-butoxycarbonylanilineHCID 22010963—

反応条件

温度85 °C

反応手順

To a solution of 2-benzyloxy-4-chlorobenzoic acid (12.9 g, 46.6 mmol), t-butanol (17.5 mL, 186 mmol) and triethylamine (7.79 mL, 55.9 mmol) in toluene (250 mL) is added DPPA (11.1 mL, 51.3 mmol) and the mixture is stirred at 85° C. for 3 h then at 65° C. for 48 h. The mixture is diluted with EtOAc (500 mL) and is washed with 1N HCl (3×150 mL), NaHCO3 (3×150 mL) and brine (150 mL). The organic phase is dried over sodium sulfate and the solvent evaporated to give a brown solid which is triturated with hexane to give the title compound: (M−1)−=332.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08084448B2
出典データセットuspto-grants-2011_12
ORD IDord-d9458652188140359ec8df881f4c9e69
出典メモuspto-grants-2011_12