반응식
[Si:1]([O:8][C@H:9]([CH2:18][O:19][Si:20]([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:22])[CH3:21])/[CH:10]=[N:11]/[S@:12]([C:14]([CH3:17])([CH3:16])[CH3:15])=[O:13])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[C:27]([Li])([CH3:30])([CH3:29])[CH3:28].C1C[O:35][CH2:34]C1>>[Si:1]([O:8][C@H:9]([CH2:18][O:19][Si:20]([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:21])[CH3:22])[C@@H:10]([NH:11][S@:12]([C:14]([CH3:15])([CH3:16])[CH3:17])=[O:13])[CH2:28][CH:27]1[CH2:30][CH2:34][O:35][CH2:29]1)([C:4]([CH3:7])([CH3:5])[CH3:6])([CH3:3])[CH3:2]참가 물질
4
반응 조건
- 온도
- -78 °C
실험 절차
A solution of azeotropically dried (S,E)-N-((S)-2,3-bis(tert-butyldimethylsilyloxy)propylidene)-2-methylpropane-2-sulfinamide (2.3 g, 5 mmol) and 3-(iodomethyl)-THF (1 g, 7 mmol) in dry THF (10 mL) was brought to −78° C. followed by the dropwise addition of tert-butyllithium (6 mL, 11 mmol). A white precipitate was formed. The resulting solution was stirred at −78° C. for 40 min, quenched with sat NH4Cl and extracted with EtOAc. The combined organics were washed with brine, dried over Na2SO4, filtered, concentrated, and chromatographed on silica gel using 0-5% EtOAc/hexanes to afford a colorless oil as (S)-N-((2S,3S)-3,4-bis(tert-butyldimethylsilyloxy)-1-(tetrahydrofuran-3-yl)butan-2-yl)-2-methylpropane-2-sulfinamide.
후처리
- customwas brought to −78° C.
- customA white precipitate was formed
- customquenched with sat NH4Cl
- extractionextracted with EtOAc
- washThe combined organics were washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customchromatographed on silica gel using 0-5% EtOAc/hexanes
출처 및 근거
- ORD 기록
- ord-5854fd72d51041fd9d5ce3afe3f767a3
- 출처 데이터셋
- uspto-grants-2013_10
- 특허 번호
- US08552181B2
연결된 노트
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