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Chloromethyl Methyl Ether → Diethyl 4-(methoxymethoxy)cyclohexane-1,1-dicarboxylate

HRID 1059298
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HRID 1059298 반응식
[OH:1][CH:2]1[CH2:7][CH2:6][C:5]([C:13]([O:15][CH2:16][CH3:17])=[O:14])([C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH2:4][CH2:3]1.C(N(C(C)C)CC)(C)C.[CH3:27][O:28][CH2:29]Cl>ClCCl>[CH3:27][O:28][CH2:29][O:1][CH:2]1[CH2:3][CH2:4][C:5]([C:8]([O:10][CH2:11][CH3:12])=[O:9])([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH2:6][CH2:7]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7864Chloromethyl Methyl EtherHCID 81531DiisopropylethylamineHCID 18670742Diethyl 4-hydroxycyclohexane-1,1-dicarboxylate

생성물 1

HCID 18670551Diethyl 4-(methoxymethoxy)cyclohexane-1,1-dicarboxylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

12.3 g of diethyl 4-hydroxycyclohexane-1,1-dicarboxylate was dissolved in 160 ml of dichloromethane and 26.3 ml of diisopropylethylamine was added thereto followed by ice-cooling. Next, 9.6 ml of chloromethyl methyl ether was added thereto and the reaction mixture was stirred at room temperature for 15 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 11.10 g of the title compound as a colorless oily substance.

후처리

  1. temperaturecooling
  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-273b8bc3c26841ec8ebd62a662593a6d
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06518423B1

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