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HRID 56469作成日:2026年10月25日

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

https://huagongshe.com/reaction/56469

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-fluorobenzoic acidHCID 40424597—
溶媒TetrahydrofuranHCID 8028—
生成物(2-Amino-5-bromo-3-fluorophenyl)methanolHCID 5431252595%

反応手順

To a solution of 2-amino-5-bromo-3-fluorobenzoic acid (14.5 g, 62.2 mmol) in THF (150 mL) at 0° C. was added borohydride in THF (1 M, 310 mL), and the reaction mixture was stirred at room temperature overnight. The reaction was quenched with methanol (150 mL), concentrated in vacuum, diluted with aqueous sodium bicarbonate (400 mL) and extracted with ethyl acetate (200 mL*3). The organic layers were separated, combined, washed with water (200 mL) and brine (200 mL), dried over sodium sulfate, filtered and concentrated to afford the title compound (13.0 g, crude), which was directly used in the next step without the further purification. MS (ES+) C7H7BrFNO requires: 219, 221, found: 220, 222 [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-cbaeea48176b456eaf135dbfa41aeec5
出典メモuspto-grants-2016_09