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Formamide → HCID 13293292, 화합물

HRID 1982427
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HRID 1982427 반응식
Br[CH:2]([CH:11](Br)[CH3:12])[C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=O.[C:14](=[O:17])([O-])[OH:15].[Na+].[CH:19]([NH2:21])=[O:20]>>[CH:14]([O:15][CH2:12][CH2:11][C:2]1[O:20][CH:19]=[N:21][C:3]=1[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 713FormamideHCID 516892Sodium BicarbonateHCID 15092305HCID 15092305, 화합물

생성물 1

HCID 13293292HCID 13293292, 화합물

실험 절차

A mixture of α,β-dibromobutyrophenone (30.6 g) and formamide (50 ml) was heated on an oil bath at 120° C.-130° C. for an hour. Then, saturated aqueous sodium hydrogen carbonate was added and the mixture was extracted with ethyl ether. The ethyl ether layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was then distilled off and the oily residue was further distilled under reduced pressure to give an oil of 5-(2-formyloxyethyl)-4-phenyloxazole, yield 12.9 g (59.4%), b.p. 136°-137° C./0.4 mmHg.

후처리

  1. temperaturewas heated on an oil bath at 120° C.-130° C. for an hour
  2. extractionthe mixture was extracted with ethyl ether
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • washThe ethyl ether layer was washed with water
  • dry with materialdried over anhydrous magnesium sulfate
  • distillationThe solvent was then distilled off
  • distillationthe oily residue was further distilled under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-7dddc510e1bd409296553de429b14301
    출처 데이터셋
    uspto-grants-1986_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04596816

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