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Ethanol → Ethyl 4-(2-nitrophenyl)-3-oxobutanoate

HRID 1833874
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반응식

HRID 1833874 반응식
C(OC(=O)C[C:6]([CH2:8][C:9](=[O:20])[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[N+:17]([O-:19])=[O:18])=[O:7])C.[CH2:22]([OH:24])[CH3:23]>>[CH2:22]([O:24][C:6](=[O:7])[CH2:8][C:9]([CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[N+:17]([O-:19])=[O:18])=[O:20])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 702EthanolHCID 131710861Ethyl-o-nitrophenylacetylacetoacetate

생성물 1

HCID 10857922Ethyl 4-(2-nitrophenyl)-3-oxobutanoate

실험 절차

30 gm (0.103M) ethyl-o-nitrophenylacetylacetoacetate was added over a period of 15-20 minutes to a saturated ammoniacal ethanol solution (prepared by bubbling NH3 gas into 400 cc. absolute for 15-20 minutes while cooling the solution to 0°-5° C.). The orangy mixture was stirred for 1 hour at 5°-10° C. and then left in the refrigerator overnight. The ethyl-γ-2-nitrophenylacetoacetate crystals formed were filtered and dried in vacuum. Additional solid was obtained after evaporation of the filtrate and washing with water to remove any amide formed.

후처리

  1. customprepared
  2. customby bubbling NH3 gas into 400 cc
  3. temperatureabsolute for 15-20 minutes while cooling the solution to 0°-5° C.)
  4. waitleft in the refrigerator overnight

출처 및 근거

ORD 기록
ord-241c7ac4eee94bf1b4527e5e78efd17d
출처 데이터셋
uspto-grants-1978_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04067871

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