Diphenyl Ether → 6-Bromo-1,4-dihydroquinolin-4-one
反応式
[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]参加物
5
実験手順
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.
後処理
- temperaturethe mixture was heated
- temperatureto reflux for 9 h
- customto afford a light brown suspension
- filtrationThen, the solids were collected by filtration
- washwashed with diethyl ether
- customAfter drying in air
出典と根拠
- ORDレコード
- ord-1e300bacd405441086d12f449fd46249
- 出典データセット
- uspto-grants-2007_08
- 特許番号
- US07253285B2
反応ノート
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