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HRID 57458作成日:2026年10月24日

4-Bromo-3-fluorobenzaldehyde → 1-(4-Bromo-3-fluorophenyl)ethan-1-ol

https://huagongshe.com/ja/reaction/57458

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromo-3-fluorobenzaldehydeHCID 2783411—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4-Bromo-3-fluorophenyl)ethan-1-olHCID 71756542—

反応手順

Methylmagnesium bromide (3M in diethylether, 6.77 mL, 20.31 mmol) was added dropwise over ˜15 min to a solution of 4-bromo-3-fluorobenzaldehyde (3.1 g, 15.27 mmol) in THF (50 mL) under argon at a temperature of −60° C. to −50° C. The ice bath was removed and the reaction mixture was allowed to warm to room temperature and stirred ˜20 hr. The reaction mixture was slowly diluted/quenched with saturated aqueous ammonium chloride solution (20 mL) and further diluted with water (10 mL). The separated aqueous layer was extracted with ethyl acetate (2×40 mL). The combined organic layers were washed with brine (60 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure to provide crude 1-(4-bromo-3-fluorophenyl)ethanol as a pale yellow oil, which was directly used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434719B2
出典データセットuspto-grants-2016_09
ORD IDord-7c6b01ce93e14c73ba9a5c6e4f2dc85a
出典メモuspto-grants-2016_09