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Pyridine → 4-(Methoxymethoxy)cyclohexane 1,1-dimethyl dimethanesulfonate

HRID 1059300
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인쇄 미리보기

반응식

HRID 1059300 반응식
[CH3:1][O:2][CH2:3][O:4][CH:5]1[CH2:10][CH2:9][C:8]([CH2:13][OH:14])(CO)[CH2:7][CH2:6]1.N1C=CC=CC=1.[CH3:21][S:22](Cl)(=[O:24])=[O:23]>ClCCl>[CH3:1][O:2][CH2:3][O:4][CH:5]1[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1.[CH3:21][S:22]([O:14][CH3:13])(=[O:24])=[O:23].[CH3:21][S:22]([O:14][CH3:13])(=[O:24])=[O:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 31297Methanesulfonyl chlorideHCID 186703154-(Methoxymethoxy)-1,1-cyclohexanedimethanol

생성물 1

HCID 865922754-(Methoxymethoxy)cyclohexane 1,1-dimethyl dimethanesulfonate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

6.84 g of 4-(methoxymethoxy)cyclohexane-1,1-dimethanol was dissolved in 110 ml of dichloromethane and 13.56 g of pyridine was added thereto and ice-cooled. 7.79 ml of methanesulfonyl chloride was added thereto and the resulting mixture was stirred at room temperature for 17 hours. Then the reaction mixture was concentrated and the residue was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate) to thereby give 11.91 g of the title compound as a colorless oily substance.

후처리

  1. temperatureice-cooled
  2. concentrationThen the reaction mixture was concentrated
  3. customthe residue was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-10eaa4b7055e4991a057692b43b4c652
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06518423B1

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