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Water → 3-Allyloxy-4,6-diacetyl-N-ethylaniline

HRID 1065115
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HRID 1065115 반응식
[CH2:1](Br)[CH:2]=[CH2:3].[C:5]([C:8]1[CH:13]=[C:12]([C:14](=[O:16])[CH3:15])[C:11]([OH:17])=[CH:10][C:9]=1[NH:18][CH2:19][CH3:20])(=[O:7])[CH3:6].C(=O)([O-])[O-].[K+].[K+].O>CN(C)C=O>[CH2:1]([O:17][C:11]1[CH:10]=[C:9]([C:8]([C:5](=[O:7])[CH3:6])=[CH:13][C:12]=1[C:14](=[O:16])[CH3:15])[NH:18][CH2:19][CH3:20])[CH:2]=[CH2:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 7841Allyl bromideHCID 11430Potassium CarbonateHCID 204815274,6-Diacetyl-3-ethylaminophenol

생성물 1

HCID 204815283-Allyloxy-4,6-diacetyl-N-ethylaniline수율 93%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Allyl bromide (2 g) was added to a stirred solution of 4,6-diacetyl-3-ethylaminophenol (0.016 M) in dimethylformamide (30 ml) containing potassium carbonate (2 g). The mixture was heated at 60°-70° C. for two hours, and was then poured into water (100 ml), stirred, and the precipitated product isolated by filtration. Yield 93%, mp 82°-83° C.

후처리

  1. temperatureThe mixture was heated at 60°-70° C. for two hours
  2. customthe precipitated product isolated by filtration

출처 및 근거

ORD 기록
ord-14afaa25679748c0adaa060c08284d90
출처 데이터셋
uspto-grants-1982_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04328341

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