Water → 2-Thienylmethyl methanesulfonate

HRID 52184

반응식

HRID 52184 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][OH:7].C(N(CC)CC)C.[CH3:15][S:16](Cl)(=[O:18])=[O:17].O>C(Cl)Cl>[CH3:15][S:16]([O:7][CH2:6][C:2]1[S:1][CH:5]=[CH:4][CH:3]=1)(=[O:18])=[O:17]

참가 물질

6

반응물 4

HCID 962WaterHCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 694672-Thiophenemethanol

생성물 1

HCID 189734302-Thienylmethyl methanesulfonate수율 38%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a 0° C. mixture of 2-thiophenemethanol (2.80 g, 24.5 mmol) and triethylamine (5.10 mL, 36.8 mmol) in CH2Cl2 (25 mL) was added methanesulfonyl chloride (2.09 mL, 27.0 mmol) and the reaction mixture was stirred for 2 hours. The reaction mixture was poured into H2O and the layers were separated. The organic phase was washed with cold 1N HCl (3×), saturated aqueous NaHCO3, and brine, dried over MgSO4, filtered. and concentrated in vacuo. 2-thienylmethyl methanesulfonate (1.78 g, 38%) was obtained by chromatography on silica gel (20% ethyl acetate/hexane).

후처리

  1. customthe layers were separated
  2. washThe organic phase was washed with cold 1N HCl (3×), saturated aqueous NaHCO3, and brine
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationand concentrated in vacuo

출처 및 근거

ORD 기록
ord-7a6e7ff6416e4d33a0570bba9e53735b
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05616596

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