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HRID 323135作成日:2026年10月27日

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

https://huagongshe.com/reaction/323135

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BenzeneHCID 241—
生成物2-benzyloxy-4-chloro-N-tert-butoxycarbonylanilineHCID 22010963—

反応手順

2-Benzyloxy-4-chlorobenzoic acid (3.0 g) was heated under reflux in a mixture of benzene and t-butyl alcohol. Diphenylphosphoryl azide (3.14 g) and triethylamine (1.21 g) were added in one batch to the mixture and reflux was continued for a further 8 hours. Benzene was removed under reduced pressure and the residue taken up in ethyl acetate. An insoluble white solid was removed by filtration. The remaining organic filtrate was washed successively with diluted hydrochloric acid, water, saturated aqueous sodium hydrogen carbonate and brine. The organic layer was dried over magnesium sulfate and the solvent was evaporated to give 2-benzyloxy-4-chloro-N-tert-butoxycarbonylaniline (1.6 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211242B1
出典データセットuspto-grants-2001_04
ORD IDord-2e09c12c1f6b4a26b67542010047bcc9
出典メモuspto-grants-2001_04