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HRID 2963作成日:2026年10月25日

Bromoacetyl bromide → N-(Benzyloxy)-2-bromoacetamide

https://huagongshe.com/reaction/2963

反応式

関与物質

役割名称HCID仕込み量
反応物Bromoacetyl bromideHCID 61147—
反応物DiisopropylethylamineHCID 81531—
反応物Benzyloxyamine hydrochlorideHCID 102312—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物N-(Benzyloxy)-2-bromoacetamideHCID 1543488652%

反応手順

To a 0° C. solution of O-benzylhydroxylamine hydrochloride (1.6 g, 10 mmol) in THF (40 mL) was added bromoacetyl bromide (871 μL, 10 mmol) and diisopropylethylamine (3.5 mL, 20 mmol). The reaction mixture was warmed to room temperature overnight and diluted with ethyl acetate and water. The aqueous layer was separated and extracted with ethyl acetate. The organic layers were combined, dried over Na2SO4, filtered and concentrated in vacuo. The crude material was purified by silica gel flash column chromatography with ethyl acetate-hexane to give 1.27 g (52%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731438
出典データセットuspto-grants-1998_03
ORD IDord-31db870c320a495ea81c261721daf508
出典メモuspto-grants-1998_03