4-Aminophenol → 1-(4-Hydroxyphenyl)-5-oxopyrrolidine-3-carboxylic acid

HRID 858920

반응식

HRID 858920 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[C:9]([OH:17])(=[O:16])[C:10]([CH2:12][C:13](O)=[O:14])=[CH2:11]>>[OH:8][C:5]1[CH:6]=[CH:7][C:2]([N:1]2[C:13](=[O:14])[CH2:12][CH:10]([C:9]([OH:17])=[O:16])[CH2:11]2)=[CH:3][CH:4]=1

참가 물질

3

반응물 2

HCID 4034-AminophenolHCID 811Itaconic acid

생성물 1

HCID 31453971-(4-Hydroxyphenyl)-5-oxopyrrolidine-3-carboxylic acid

실험 절차

A mixture of 2.355 mol of 4-aminophenol and 2.32 mol of itaconic acid was heated gradually: At 60° C., the powder started to become viscous, at 110–120° C. it became liquid and the colour turned to dark brown while the rest of solid material was also dissolved. The exothermic reaction started under boiling, and the temperature rose to 150° C. The sandy product was left to cool down to RT within 1–2 hours. The obtained crude (RS)-1-(4-hydroxyphenyl)-5-oxo-pyrrolidine-3-carboxylic acid was engaged in the next step without further purification or characterisation.

후처리

  1. temperaturewas heated gradually
  2. customAt 60° C.
  3. customto become viscous, at 110–120° C.
  4. dissolutionwas also dissolved
  5. customThe exothermic reaction
  6. customrose to 150° C
  7. waitThe sandy product was left

출처 및 근거

ORD 기록
ord-a66ee9f001084ccf87d53c96ee09a8e2
출처 데이터셋
uspto-grants-2006_12
특허 번호
US07148362B2

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