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Methanol → 2-bromo-1-(2-hydroxy-phenyl)-ethanone O-methyl-oxime

HRID 2289870
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인쇄 미리보기

반응식

HRID 2289870 반응식
[Br:1][CH:2](O)[C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=O.Cl.[CH3:13][O:14][NH2:15].C[OH:17]>>[CH3:13][O:14][N:15]=[C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[OH:17])[CH2:2][Br:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 521874O-Methylhydroxylamine hydrochlorideHCID 222371692-Bromo-2-hydroxy-1-phenylethan-1-one

생성물 1

HCID 1359803292-bromo-1-(2-hydroxy-phenyl)-ethanone O-methyl-oxime수율 52%

반응 조건

온도
0 °C

실험 절차

107.5 g (0.5 mol) of ω-bromo-2-hydroxy-acetophenone in 500 ml of methanol together with 41.75 g (0.5 mol) of O-methylhydroxylamine hydrochloride are heated under reflux for 4 hours. The methanol is distilled off under reduced pressure and the residue is admixed with 500 ml of water and extracted with 4 times 100 ml of ethyl acetate. The organic phase is dried over sodium sulphate and the solvent is distilled off under reduced pressure. At 0° C., the residue is stirred with petroleum ether, affording 74 g (52% of theory) of crystalline 2-bromo-1-(2-hydroxy-phenyl)-ethanone O-methyl-oxime as a mixture of two stereoisomers (53% of isomer B and 33% of isomer A).

후처리

  1. temperatureunder reflux for 4 hours
  2. distillationThe methanol is distilled off under reduced pressure
  3. extractionextracted with 4 times 100 ml of ethyl acetate
  4. dry with materialThe organic phase is dried over sodium sulphate
  5. distillationthe solvent is distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-8062db1e601449ee804880fc5fe0a11b
출처 데이터셋
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06093837

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