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Diphenyl Ether → 6-Bromo-1,4-dihydroquinolin-4-one

HRID 852983
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HRID 852983 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][C:6](C(O)=O)=[C:5]2[OH:15].C1(OC2C=CC=CC=2)C=CC=CC=1>CO.C(OCC)C>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][CH:6]=[C:5]2[OH:15]
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참가 물질

5

반응물 2

HCID 7583Diphenyl EtherHCID 178524706HCID 178524706, 화합물

생성물 1

HCID 1785163796-Bromo-1,4-dihydroquinolin-4-one수율 95.7%

시약·촉매·용매 2

HCID 887Methanol용매HCID 3283Diethyl Ether용매

실험 절차

The solid 6-bromo-4-hydroxy-quinoline-3-carboxylic acid (102.59 g, 337.7 mmol) was added to hot diphenyl ether (508 g) and then the mixture was heated to reflux for 9 h to afford a light brown suspension. After cooling to room temperature, the mixture was diluted with methanol (20 mL) and diethyl ether (300 mL). Then, the solids were collected by filtration and washed with diethyl ether. After drying in air, 72.43 g (95% yield) of 6-bromo-quinolin-4-ol was isolated as a white solid: EI-HRMS m/e calcd for C9H6BrNO (M+) 222.9633, found 222.9630.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 9 h
  3. customto afford a light brown suspension
  4. filtrationThen, the solids were collected by filtration
  5. washwashed with diethyl ether
  6. customAfter drying in air

출처 및 근거

ORD 기록
ord-1e300bacd405441086d12f449fd46249
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07253285B2

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