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Ozone → 2-Hydroxy-3-(o-tolylthio)benzaldehyde

HRID 1164106
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HRID 1164106 반응식
[O:1]=[O+][O-].[C:4]1([CH3:21])[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10][C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([CH:17]=CC)[C:12]=1[OH:20]>C(OCC)(=O)C.C(O)(=O)C>[OH:20][C:12]1[C:11]([S:10][C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[CH3:21])=[CH:16][CH:15]=[CH:14][C:13]=1[CH:17]=[O:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24823OzoneHCID 544721892-(o-Tolylthio)-6-(1-propenyl)phenol

생성물 1

HCID 130666712-Hydroxy-3-(o-tolylthio)benzaldehyde

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 8857Ethyl Acetate용매

실험 절차

Ozone gas was introduced into a solution of 2-(o-tolylthio)-6-(1-propenyl)phenol (24.3 g) in a mixture of ethyl acetate (200 ml) and acetic acid (5 ml) at 3° C. for 1.5 hours. The excess of ozone was removed by air-bubbling and further decomposed with aqueous sodium hydrogen sulfite. The resultant organic layer was separated, washed with aqueous sodium hydrogen sulfite and water in turn, dried and then evaporated under reduced pressure. The oily residue was crystallized with ethanol to give yellow needles of 2-hydroxy-3-(o-tolylthio)benzaldehyde (12.2 g), mp. 42°-43° C.

후처리

  1. customThe excess of ozone was removed
  2. customby air-bubbling
  3. customThe resultant organic layer was separated
  4. washwashed with aqueous sodium hydrogen sulfite and water in turn
  5. customdried
  6. customevaporated under reduced pressure
  7. customThe oily residue was crystallized with ethanol

출처 및 근거

ORD 기록
ord-6041813b2ee9438fb4c0a85aaaca0a6e
출처 데이터셋
uspto-grants-1983_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04367238

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