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HRID 324456作成日:2026年10月26日

Dimethylformamide → (3-Ethylphenyl)methanol

https://huagongshe.com/reaction/324456

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—
溶媒TetrahydrofuranHCID 8028—
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 tetrahydrofuran (320 ml) at −78° C. After 1 hour N,N-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06218376B1
出典データセットuspto-grants-2001_04
ORD IDord-7614c6145c424c9396a8ab177d39f1fb
出典メモuspto-grants-2001_04