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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131753생성일: 2026년 10월 26일

p-Bromobenzenesulfonyl chloride → (S)-(-)-3-Chloro-1-phenyl-1-propanol

https://huagongshe.com/reaction/131753

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참여 물질

역할이름HCID투입량
반응물p-Bromobenzenesulfonyl chlorideHCID 7396—
반응물TriethylamineHCID 8471—
반응물(1S)-1-phenylpropane-1,3-diolHCID 6950537—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매tert-Butyl methyl etherHCID 15413—
생성물(S)-(-)-3-Chloro-1-phenyl-1-propanolHCID 2777894114.1%

반응 조건

온도0 °C

반응 단계

To a solution of (S)-1-phenyl-1,3-propanediol (125 g, 0.822 mole) in methyl tert-butyl ether (500 mL) was added triethylamine (135 mL). The reaction mixture was cooled to 0° C. and a solution of 4-bromobenzenesulfonyl chloride (230 g, 0.92 mole) in methyl tert-butyl ether (300 mL) and tetrahydrofuran (300 mL) was added dropwise over 3 hour. After the addition, the reaction mixture was stirred at 0° C. for three hours and was then warmed to ambient temperature. After stirring at ambient temperature for 18 hours, benzyltriethylammonium chloride (210 g, 0.92 mole) was added and the resulting mixture was heated at 55° C. for three hours. The reaction mixture was cooled to ambient temperature and then diluted with water. After separation of the organic phase, the aqueous phase was extracted two times with diethyl ether. The combined organic extracts were washed with 1.0 N hydrochloric acid, saturated aqueous sodium bicarbonate, water, saturated aqueous sodium chloride, dried over magnesium sulfate, and concentrated under reduced pressure to provide an off-white solid (160 g). This solid was subjected to silica gel chromatography, eluting with ethyl acetate/hexane (1:9) to provide 110 grams (80%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384983B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-9e64c978b7c34c759244a14dd0dc8ba0
출처 메모uspto-grants-2008_06