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Dimethylformamide → 3-Benzylmercapto-4-chlorocarbonyl benzaldehyde

HRID 2072305
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반응식

HRID 2072305 반응식
[CH2:1]([S:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][C:16]=1[C:17]([OH:19])=O)[CH:12]=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)([Cl:22])=O.CN(C)C=O>C(Cl)Cl>[CH2:1]([S:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][C:16]=1[C:17]([Cl:22])=[O:19])[CH:12]=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 539168353-Benzylmercapto-4-carboxy benzaldehyde

생성물 1

HCID 536823133-Benzylmercapto-4-chlorocarbonyl benzaldehyde

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution containing 23.2 g of 3-benzylmercapto-4-carboxy benzaldehyde in 250 ml of methylene chloride is added 15 ml of thionyl chloride and 0.5 ml of dimethylformamide. The reaction mixture is refluxed for 6-7 hours, then evaporated to dryness. Crystallization from 100 ml of ether yielded 27.0 g of 3-benzylmercapto-4-chlorocarbonyl benzaldehyde (a).

후처리

  1. temperatureThe reaction mixture is refluxed for 6-7 hours
  2. customevaporated to dryness
  3. customCrystallization from 100 ml of ether

출처 및 근거

ORD 기록
ord-44e2cdc2638042c2b7194d606af3c913
출처 데이터셋
uspto-grants-1977_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04051148

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