반응식
[O:1]1[CH2:6][CH2:5][CH2:4][CH:3]([CH2:7][OH:8])[CH2:2]1.C(N(CC)CC)C.[S:16](Cl)([CH3:19])(=[O:18])=[O:17]>ClCCl>[CH3:19][S:16]([O:8][CH2:7][CH:3]1[CH2:4][CH2:5][CH2:6][O:1][CH2:2]1)(=[O:18])=[O:17]참가 물질
5
실험 절차
To tetrahydro-2H-pyran-3-ylmethanol (4.92 g) in dry dichloromethane (140 ml) at 0° C. and under nitrogen, was added anhydrous triethylamine (13.6 ml) in one go, followed by mesyl chloride (4.3 ml) dropwise over 5 minutes. The reaction was allowed to warm to room temperature and stirred at this temperature overnight. The reaction was quenched with saturated aqueous sodium bicarbonate (50 ml). The organic layer was separated, passed through a hydrophobic frit to dry and concentrated in vacuo to yield a red oil (8.8 g).
후처리
- customThe reaction was quenched with saturated aqueous sodium bicarbonate (50 ml)
- customThe organic layer was separated
- customto dry
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-da1ea2a94585412492498f6165dd4248
- 출처 데이터셋
- uspto-grants-2011_07
- 특허 번호
- US07977344B2
연결된 노트
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