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4-Chlorobenzamide → HCID 22761225, 화합물

HRID 1703437
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HRID 1703437 반응식
[C:1]([C:5]([CH:7]=[O:8])=[O:6])([CH3:4])([CH3:3])[CH3:2].[Cl:9][C:10]1[CH:18]=[CH:17][C:13]([C:14]([NH2:16])=[O:15])=[CH:12][CH:11]=1>C1C=CC=CC=1>[Cl:9][C:10]1[CH:18]=[CH:17][C:13]([C:14]([NH:16][CH:7]([OH:8])[C:5](=[O:6])[C:1]([CH3:4])([CH3:3])[CH3:2])=[O:15])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 120844-ChlorobenzamideHCID 3499723,3-Dimethyl-2-oxobutanal

생성물 1

HCID 22761225HCID 22761225, 화합물수율 54%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

14 g (0.123 mol) of freshly distilled tert.-butylglyoxal were dissolved in 150 ml of absolute benzene. 19.1 g (0.123 mol) of p-chlorobenzamide were added and the mixture was heated for 15 hours under reflux. On cooling, the reaction product crystallised out. 16.1 g (54% of theory) of 1-(p-chlorobenzamido)-3,3-dimethyl-1-hydroxy-butan-2-one of melting point 130° C. were obtained.

후처리

  1. temperaturethe mixture was heated for 15 hours
  2. temperatureunder reflux
  3. temperatureOn cooling
  4. customthe reaction product crystallised out

출처 및 근거

ORD 기록
ord-f25c3edfbcd64ca7aa0a87f5e4bf8059
출처 데이터셋
uspto-grants-1978_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04124369

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