반응식
[CH3:1][CH:2]([OH:11])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].C(N(C(C)C)CC)(C)C.[CH3:21][S:22](Cl)(=[O:24])=[O:23].Cl>C(Cl)Cl>[CH3:21][S:22]([O:11][CH:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[CH3:1])(=[O:24])=[O:23]참가 물질
실험 절차
To a solution of 2-decanol (5.0 ml, 26.0 mmol) in dry CH2Cl2 (52 ml) under an N2 atmosphere was added diisopropylethylamine (5.6 ml, 32.1 mmol). The reaction flask was immersed in an ice/water bath. After stirring for 10 minutes, methanesulfonyl chloride (2.8 ml, 36.1 mmol) was added via syringe over a period of 10 minutes. After stirring for 3 hrs, the reaction was diluted with cold CH2Cl2 (200 ml) and poured into cold 5% aqueous HCl (100 ml). The layers were separated and the organic phase washed with cold 5% aqueous HCl (50 ml) followed by brine (2×50 ml). The CH2Cl2 layer was dried (Na2SO4), filtered and evaporated in vacuo at 25° C. The resulting light yellow oil was pumped under reduced pressure for 2 hrs to provide 2-methanesulfonyloxydecane (6.5 g, 93.5%) as a light yellow oil.
후처리
- customThe reaction flask was immersed in an ice/water bath
- stirringAfter stirring for 3 hrs
- customThe layers were separated
- washthe organic phase washed with cold 5% aqueous HCl (50 ml)
- dry with materialThe CH2Cl2 layer was dried (Na2SO4)
- filtrationfiltered
- customevaporated in vacuo at 25° C
- waitThe resulting light yellow oil was pumped under reduced pressure for 2 hrs
출처 및 근거
- ORD 기록
- ord-5a1d40dd5fcf4d18bba31938757d23a5
- 출처 데이터셋
- uspto-grants-1997_03
- 특허 번호
- US05607660
연결된 노트
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