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HRID 241517作成日:2026年10月27日

Water → 4-bromo-3-chloro-N-trimethylsilanylmethyl-benzamide

https://huagongshe.com/reaction/241517

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-(Trimethylsilyl)methylamineHCID 87488—
反応物4-Bromo-3-chlorobenzoic acidHCID 12594302—
溶媒DichloromethaneHCID 6344—
生成物4-bromo-3-chloro-N-trimethylsilanylmethyl-benzamideHCID 66836699100%

反応条件

温度20 °C

反応手順

To a suspension of 4-bromo-3-chlorobenzoic acid (25.00 g, 106.2 mmol) in CH2Cl2 (320 mL) was added N,N-dimethyl aminopyridine (1.95 g), followed by N-ethyl-N-dimethylamine propylcarbodiimide hydrochloride (22.39 g) in small portions. After 30 min at room temperature, aminomethyl trimethylsilane (11.2 g, 7.87 mL, 108 mmol) was added while maintaining the temperature at 20° C. After stirring over night, water was added and the organic layer was separated. The aqueous layer was extracted twice with CH2Cl2 and the combined organic phases were dried and evaporated in vacuum. The residue was purified by flash chromatography on silica gel to give the title compound (34.00 g, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653000B2
出典データセットuspto-grants-2014_02
ORD IDord-e86fb4dcd46743ff948c85722bfc7573
出典メモuspto-grants-2014_02