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HRID 748748作成日:2026年10月24日

Hexane → 1-(2,5-Difluorophenyl)-5-(methylsulfonyl)-1-pentanol

https://huagongshe.com/ja/reaction/748748

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物2-Bromo-1,4-difluorobenzeneHCID 67862—
反応物5-MethanesulfonylpentanalHCID 23028565—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物1-(2,5-Difluorophenyl)-5-(methylsulfonyl)-1-pentanolHCID 2302855237.8%

反応手順

A tetrahydrofuran (5 ml) solution of 1-bromo-2,5-difluorobenzene (0.151 ml, 1.34 mmol) was stirred at −78° C. To the resulting mixture was added a hexane solution (0.843 ml, 1.34 mmol) of n-butyl lithium. The reaction mixture was added to a tetrahydrofuran (5 ml) solution of 5-(methylsulfonyl)pentanal (183 mg, 1.11 mmol) at −78° C. and at the same temperature, stirring was conducted for 30 minutes. After elevating the temperature of the reaction mixture to room temperature, diethyl ether was added thereto. The resulting mixture was washed successively with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium bicarbonate. The organic layer was then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was subjected to flash silica gel chromatography, and the fraction obtained from the hexane:ethyl acetate=1:2 eluate was concentrated under reduced pressure, whereby the title compound (116 mg, 0.42 mmol, 37%) was obtained as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07399775B2
出典データセットuspto-grants-2008_07
ORD IDord-3bc77660a3234e9bbd149703a1a2777c
出典メモuspto-grants-2008_07