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HRID 132644作成日:2026年10月26日

Tetrahydrofuran → (S)-2-(2,4-Difluoro-benzyl)-butan-1-ol

https://huagongshe.com/reaction/132644

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Sodium borohydrideHCID 4311764—
反応物(4R,5S)-[(S)-2-(2,4-Difluoro-benzyl)-butyryl]-4-methyl-5-phenyl-oxazolidin-2-oneHCID 69267273—
溶媒WaterHCID 962—
生成物(S)-2-(2,4-Difluoro-benzyl)-butan-1-olHCID 6927100946%

反応条件

温度0 °C

反応手順

A flask was charged with 29.5 g (˜78.6 mmol) of (4R,5S)-[(S)-2-(2,4-difluoro-benzyl)-butyryl]-4-methyl-5-phenyl-oxazolidin-2-one and 200 mL of dry THF, and the solution was cooled to 0° C. In a separate flask, 11.9 g (314 mmol) of sodium borohydride was taken up in 70 mL of water and added dropwise over 15 minutes to the imide solution. The mixture was allowed to warm to room temperature and stirred overnight. The reaction mixture was quenched with conc. HCl until pH=3 (keeping the reaction mixture temperature <20° C.). THF was removed under reduced pressure, and the residue was taken up in hexanes. The hexane layer was washed with sat. aq. sodium bicarbonate. The hexane layer was removed under reduced pressure, and the residue was purified by column chromatography (9:1 Hexanes/EtOAc) which gave 7.2 g (46% yield) of the titled compound as a clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07388023B2
出典データセットuspto-grants-2008_06
ORD IDord-22135f04b12543578b387fd66baa32ae
出典メモuspto-grants-2008_06