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HRID 1871981作成日:2026年10月24日

Dimethylformamide → (3-Ethylphenyl)methanol

https://huagongshe.com/ja/reaction/1871981

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Benzene, 1-bromo-3-ethyl-HCID 123170—
反応物ButyllithiumHCID 178418339—
生成物(3-Ethylphenyl)methanolHCID 104659—

反応条件

温度-78 °C

反応手順

n-Butyllithium (34 ml of a 2.5M solution in hexanes) was added to a solution of 1-bromo-3-ethylbenzene (15 g) in tetrahydrofuiran (320 ml) at -78° C. After 1 hour dimethylformamide (15 ml) was added. The mixture was stirred at -78° C. for 1 hour and allowed to warm to room temperature. The mixture was quenched with aqueous ammonium chloride and partitioned between ethyl acetate and water. The organic phase was dried (MgSO4) and evaporated. The residue was dissolved in methanol (250 ml) and treated with sodium borohydride (1.51 g) portionwise. The mixture was stirred at room temperature for 16 hours, quenched with 2M HCl (100 ml) and stirred for 4 hours. The mixture was concentrated under reduced pressure and the residue partitioned between ethyl acetate and 2M HCl. The organic phase was dried (MgSO4), evaporated and the residue purified by chromatography eluting with 5-10% ethyl acetate in isohexane. Yield 7.6 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06107297
出典データセットuspto-grants-2000_08
ORD IDord-67c0ade42e234dbc896845d69eedfce8
出典メモuspto-grants-2000_08