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Acetonitrile → HCID 672273, 화합물

HRID 425256
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HRID 425256 반응식
[OH-].[K+].[NH2:3][C:4]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:5]=1[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)=O.C(OCC)(=O)C.[C:25](#[N:27])[CH3:26]>>[NH2:27][C:25]1[CH:26]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:5]2[C:4](=[CH:17][CH:16]=[C:15]([Cl:18])[CH:14]=2)[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6342Acetonitrile2회HCID 8857Ethyl AcetateHCID 128702-Amino-5-chlorobenzophenoneHCID 14797Potassium Hydroxide

생성물 1

HCID 672273HCID 672273, 화합물

실험 절차

A suspension of 1.4 g of powdered KOH in 25 ml of anhydrous acetonitrile stirred under an argon atmosphere was heated to boiling under reflux conditions for 30 minutes and then a solution of 1.15 g of 2-amino-5-chlorobenzophenone in 5 ml of anhydrous acetonitrile was added. The mixture was boiled with a reflux condenser for 12 hours. Cooling was followed by pouring into ice, extraction with ethyl acetate, washing with water and removal of the solvent by distillation.

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후처리

  1. temperaturewas heated
  2. waitThe mixture was boiled with a reflux condenser for 12 hours
  3. temperatureCooling
  4. washwashing with water and removal of the solvent by distillation

출처 및 근거

ORD 기록
ord-7dc9ff98ac3644f5a21d8a9e0abb0b06
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106204B2

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