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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 901076생성일: 2026년 10월 26일

(Diethylamino)sulfur trifluoride → tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(fluoromethylthio)phenyl]-1,3-oxazolidine-3-carboxylate

https://huagongshe.com/reaction/901076

반응식

참여 물질

역할이름HCID투입량
반응물(Diethylamino)sulfur trifluorideHCID 123472—
반응물Sodium BicarbonateHCID 516892—
반응물tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(methylsulfinyl)phenyl]-1,3-oxazolidine-3-carboxylateHCID 68720168—
촉매Antimony trichlorideHCID 24814—
용매DichloromethaneHCID 6344—
생성물tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(fluoromethylthio)phenyl]-1,3-oxazolidine-3-carboxylateHCID 6871963986.5%

반응 단계

A solution of diethylamino sulfurtrifluoride (DAST), (9.34 g, 1.75 eq ) in 10 ml of dichloromethane was added drop wise to the solution of 14 (12.3 g) and antimony (III) chloride (0.23 g, 0.03 eq ) in 150 ml of dichloromethane (anhydrous) at −5° C., and the reaction mixture was warmed up to room temperature overnight. A cold saturated solution of sodium bicarbonate (80 ml) was added and stirred for 30 min and extracted with dichloromethane (100 ml×2). The organic layer was washed with a 10% solution of sodium bicarbonate and with brine (50 ml) and dried over sodium sulfate. After purification, via a column, 10.7 g of the desired product (as a heavy oil) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07361689B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-ebb033e654d74be2a94b18917bab6ff1
출처 메모uspto-grants-2008_04