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Ethanol → Ethyl 2-phenylthiazole-5-carboxylate

HRID 2301870
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반응식

HRID 2301870 반응식
[CH:1]([CH:3](Cl)[C:4]([O-:6])=[O:5])=O.[C:8]([NH2:16])(=[S:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH3:17][CH2:18]O>>[CH2:17]([O:6][C:4]([C:3]1[S:15][C:8]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[N:16][CH:1]=1)=[O:5])[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 683563ThiobenzamideHCID 22350456HCID 22350456, 화합물

생성물 1

HCID 9899456Ethyl 2-phenylthiazole-5-carboxylate수율 15%

실험 절차

A solution of α-formyl-α-chloroacetate (9.34 g, 49.5 mmol, 1 eq) and thiobenzamide (6.79 g, 49.5 mmol, 1 eq) in EtOH (37.0 mL) is refluxed for 1 hour. The solution changes from an orange/brown color to a deep green. This solution is washed with water and extracted with CH2Cl2. The organic fraction is dried over Na2SO4, filtered, and the solvent removed in vacuo. The product is purified by column chromatography using a Biotage Flash 40M column (20% hexanes/EtOAc) to give the product as,a deep orange oil (1.82 g, 15%). MS (ESI) for C12H13NO3S m/z 252.1 (M+H)+.

후처리

  1. wash
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
This solution is washed with water
  • extractionextracted with CH2Cl2
  • dry with materialThe organic fraction is dried over Na2SO4
  • filtrationfiltered
  • customthe solvent removed in vacuo
  • customThe product is purified by column chromatography
  • 출처 및 근거

    ORD 기록
    ord-2e8c4d1d9ccb4e11b5ef7958de71630f
    출처 데이터셋
    uspto-grants-2002_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06500840B2

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