Water → HCID 53699063, 화합물

HRID 1679070노트

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HRID 1679070 반응식
[N+]([O-])([O-])=O.[NH4+].[Ce+4].[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.[N+]([O-])([O-])=O.[OH2:23].[CH2:24]([O:26][C:27]([C:29]1[O:30][C:31]([C:38]2[CH:43]=[CH:42][C:41]([Cl:44])=[CH:40][CH:39]=2)=[C:32]2[C:37]=1[CH:36]=[CH:35][CH:34]=[CH:33]2)=[O:28])[CH3:25]>C(O)(=O)C>[CH2:24]([O:26][C:27](=[O:28])[C:29]([C:37]1[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=1[C:31](=[O:30])[C:38]1[CH:43]=[CH:42][C:41]([Cl:44])=[CH:40][CH:39]=1)=[O:23])[CH3:25]

참가 물질

5

실험 절차

11.5 G. of cerium (IV) ammonium nitrate are dissolved in 20 ml. of water and 20 ml. of glacial acetic acid. Thereafter, there are added 3.0 g. of 3-(p-chlorophenyl)-isobenzofuran-1-carboxylic acid ethyl ester and the mixture is boiled for 2-3 minutes until the color of the solution obtained changes from orange to light-yellow. After cooling, there are added 150 ml. of ice-water and the mixture is stirred for 1 hour in an ice-bath. The product which first separates as an oil solidifies. The solid is separated by decantation of the aqueous solution and is dissolved in ether. The ethereal solution is washed with 2-N sodium carbonate and water, dried over sodium sulfate and evaporated. After crystallization of the residue from ethanol, there is obtained [o-(p-chlorobenzoyl)-phenyl]glyoxylic acid ethyl ester in the form of colorless crystals having a melting point of 79°-81° C.

후처리

  1. additionThereafter, there are added 3.0 g
  2. customobtained changes from orange to light-yellow
  3. temperatureAfter cooling
  4. additionthere are added 150 ml
  5. customThe solid is separated by decantation of the aqueous solution
  6. dissolutionis dissolved in ether
  7. washThe ethereal solution is washed with 2-N sodium carbonate and water
  8. dry with materialdried over sodium sulfate
  9. customevaporated
  10. customAfter crystallization of the residue from ethanol

출처 및 근거

ORD 기록
ord-b593d72c65074d17a5dad06f363b9ce6
출처 데이터셋
uspto-grants-1978_03
특허 번호
US04077978

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