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4,5-Bis(4-methoxyphenyl)-2-hydroxymethylthiazole → 4,5-Bis(4-methoxyphenyl)-2-formylthiazol

HRID 1587400
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인쇄 미리보기

반응식

HRID 1587400 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:10]=[C:11]([CH2:22][OH:23])[S:12][C:13]=2[C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)=[CH:5][CH:4]=1>C(OCC)(=O)C.[O-2].[O-2].[Mn+4]>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[N:10]=[C:11]([CH:22]=[O:23])[S:12][C:13]=2[C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 103365644,5-Bis(4-methoxyphenyl)-2-hydroxymethylthiazole

생성물 1

HCID 103816794,5-Bis(4-methoxyphenyl)-2-formylthiazol수율 64.9%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 4,5-bis(4-methoxyphenyl)-2-hydroxymethylthiazole (5.04 g) and manganese dioxide (35.0 g) in ethyl acetate (250 ml) was stirred at ambient temperature for 5.5 hours. After filtration, the filtrate was evaporated in vacuo, and the resulting residue was washed with hexane to give 4,5-bis(4-methoxyphenyl)-2-formylthiazol (3.25 g).

후처리

  1. filtrationAfter filtration
  2. customthe filtrate was evaporated in vacuo
  3. washthe resulting residue was washed with hexane

출처 및 근거

ORD 기록
ord-b2cd37ade36846708ae015591742f14c
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05217971

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