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1-(Chloromethoxy)-2-methoxyethane → 3-[1-(Methoxyethoxymethoxy)propyl]-2-methylthiothiophene

HRID 1651641
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인쇄 미리보기

반응식

HRID 1651641 반응식
[OH:1][CH:2]([C:5]1[CH:9]=[CH:8][S:7][C:6]=1[S:10][CH3:11])[CH2:3][CH3:4].[CH3:12][O:13][CH2:14][CH2:15][O:16][CH2:17]Cl.C(N(CC)C(C)C)(C)C>C(Cl)Cl>[CH3:12][O:13][CH2:14][CH2:15][O:16][CH2:17][O:1][CH:2]([C:5]1[CH:9]=[CH:8][S:7][C:6]=1[S:10][CH3:11])[CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 775901-(Chloromethoxy)-2-methoxyethaneHCID 81531DiisopropylethylamineHCID 147003823-(1-Hydroxypropyl)2-methylthiothiophene

생성물 1

HCID 147003833-[1-(Methoxyethoxymethoxy)propyl]-2-methylthiothiophene수율 94%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of 3-(1-hydroxypropyl)2-methylthiothiophene (17.7 g, 0.094 mol) in dry methylene chloride (100 ml) was added methoxyethoxymethyl chloride (20.6 g, 0.165 mol) followed by N,N,-diisopropylethylamine (21.3 g, 0.165 mol). The mixture was stirred at room temperature overnight. The mixture was washed with water, dried over anhydrous Na2SO4, filtered and concentrated in vacuo at room temperature to give 24.4 g of amber oil (94% yield). NMR confirmed the structure and mass spectral analysis confirmed the molecular weight at 276.09.

후처리

  1. washThe mixture was washed with water
  2. dry with materialdried over anhydrous Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo at room temperature

출처 및 근거

ORD 기록
ord-8423d97c6b3a4903b61957a607ae8d36
출처 데이터셋
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04929637

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