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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 748748생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물2-Bromo-1,4-difluorobenzeneHCID 67862—
반응물5-MethanesulfonylpentanalHCID 23028565—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(2,5-Difluorophenyl)-5-(methylsulfonyl)-1-pentanolHCID 2302855237.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07399775B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-3bc77660a3234e9bbd149703a1a2777c
출처 메모uspto-grants-2008_07