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

HRID 1164106
ノート
印刷プレビュー

反応式

HRID 1164106 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 8857Ethyl Acetate溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-6041813b2ee9438fb4c0a85aaaca0a6e
出典データセット
uspto-grants-1983_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04367238

反応ノート

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