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Water → 1-(4-Amino-3-nitrophenyl)-2-bromopropan-1-one

HRID 1517193
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인쇄 미리보기

반응식

HRID 1517193 반응식
[Br:1][CH:2]([CH3:18])[C:3]([C:5]1[CH:10]=[CH:9][C:8]([NH:11]C(=O)C)=[C:7]([N+:15]([O-:17])=[O:16])[CH:6]=1)=[O:4].O>Br>[NH2:11][C:8]1[CH:9]=[CH:10][C:5]([C:3](=[O:4])[CH:2]([Br:1])[CH3:18])=[CH:6][C:7]=1[N+:15]([O-:17])=[O:16]
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참가 물질

4

반응물 2

HCID 962WaterHCID 59569023N-[4-(2-bromopropanoyl)-2-nitrophenyl]acetamide

생성물 1

HCID 595690141-(4-Amino-3-nitrophenyl)-2-bromopropan-1-one수율 353.6%

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

반응 조건

온도
120 °C

실험 절차

11.65 g (37 mM) of N-[4-(2-bromopropanoyl)-2-nitrophenyl]acetamide dissolved in aqueous 47% hydrobromic acid solution are maintained at 120° C. for 15 minutes with stirring. The reaction medium is then poured into water and extracted with ethyl acetate. The organic phase is washed with water, with aqueous sodium hydrogen carbonate solution and finally with saturated aqueous sodium chloride solution. The organic phase is separated out by settling, dried over anhydrous sodium sulfate and then evaporated under vacuum to give 35.7 g of 1-(4-amino-3-nitrophenyl)-2-bromopropan-1-one in the form of a yellow solid.

후처리

  1. extractionextracted with ethyl acetate
  2. washThe organic phase is washed with water, with aqueous sodium hydrogen carbonate solution and finally with saturated aqueous sodium chloride solution
  3. customThe organic phase is separated out
  4. dry with materialdried over anhydrous sodium sulfate
  5. customevaporated under vacuum

출처 및 근거

ORD 기록
ord-22bec6d5db21480b81aa8e435adf640d
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08232272B2

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