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Water → Cycloheptylmethyl methanesulfonate

HRID 1739740
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HRID 1739740 반응식
[CH:1]1([CH2:8][OH:9])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(N(CC)CC)C.[CH3:17][S:18](Cl)(=[O:20])=[O:19].O>ClCCl>[CH3:17][S:18]([O:9][CH2:8][CH:1]1[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1)(=[O:20])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 78193Cycloheptanemethanol

생성물 1

HCID 21866479Cycloheptylmethyl methanesulfonate수율 103%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To a solution of cycloheptylmethanol (1.0 g, 7.81 mmol) in dichloromethane (20 ml) at 0° C. under nitrogen was added triethylamine (1.63 ml, 1.5 mol. equiv.) Methanesulphonyl chloride (0.73 ml, 1.2 mol. equiv.) was added, dropwise, and the reaction allowed to stir for two hours at room temperature. Water (50 ml) and dichloromethane (50 ml) were added. The organic phase was separated, washed with water (2×50 ml) and then dried over anhydrous magnesium sulphate. The solution was then filtered and the solvent removed under reduced pressure to give the title compound as an oil (1.66 g).

후처리

  1. additionwas added
  2. customThe organic phase was separated
  3. washwashed with water (2×50 ml)
  4. dry with materialdried over anhydrous magnesium sulphate
  5. filtrationThe solution was then filtered
  6. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-80caafe921d74b35bf3c6b05b6cddaf8
출처 데이터셋
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05968923

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