Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
(Diethylamino)sulfur trifluoride → tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(fluoromethylthio)phenyl]-1,3-oxazolidine-3-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(methylsulfinyl)phenyl]-1,3-oxazolidine-3-carboxylate | HCID 68720168 | — |
| 촉매 | Antimony trichloride | HCID 24814 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(fluoromethylthio)phenyl]-1,3-oxazolidine-3-carboxylate | HCID 68719639 | 86.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07361689B2 |
| 출처 데이터셋 | uspto-grants-2008_04 |
| ORD ID | ord-ebb033e654d74be2a94b18917bab6ff1 |
| 출처 메모 | uspto-grants-2008_04 |