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HRID 56448作成日:2026年10月25日

Borohydride → (2-Amino-5-bromo-3-chlorophenyl)methanol

https://huagongshe.com/reaction/56448

反応式

関与物質

役割名称HCID仕込み量
反応物BorohydrideHCID 28123—
反応物2-Amino-5-bromo-3-chlorobenzoic acidHCID 827979—
溶媒TetrahydrofuranHCID 8028—
生成物(2-Amino-5-bromo-3-chlorophenyl)methanolHCID 6708068482%

反応手順

To a solution of 2-amino-5-bromo-3-chlorobenzoic acid (13.0 g, 52.0 mmol) in THF (200 mL) was added borohydride in THF (300 mL, 1N) at ice/water bath, and the reaction mixture was stirred at room temperature overnight. The mixture was quenched with methanol (100 mL) and concentrated to a volume of 50 mL. The residue was diluted with aqueous sodium bicarbonate (400 mL) and extracted with ethyl acetate (200 mL×3). The organic layers were separated, combined, washed by brine (100 mL), dried over sodium sulfate, filtered and concentrated to afford the title product (10.0 g, 82%). MS (ES+) C7H7BrClNO requires: 234, 236, found: 236, 238 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434700B2
出典データセットuspto-grants-2016_09
ORD IDord-2c837e710ae1411eb1a34020b955fe70
出典メモuspto-grants-2016_09