N-(2-Bromophenyl)cinnamamide → 8-Bromo-1,2-dihydroquinolin-2-one

HRID 1056052

反応式

HRID 1056052 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[Br:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[NH:12][C:13](=[O:22])[CH:14]=[CH:15]C1C=CC=CC=1>ClC1C=CC=CC=1>[Br:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:7]=1[NH:12][C:13](=[O:22])[CH:14]=[CH:15]2

参加物

4

反応物 2

HCID 764332N-(2-Bromophenyl)cinnamamideHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 109330948-Bromo-1,2-dihydroquinolin-2-one収率 67.2%

試薬・触媒・溶媒 1

HCID 7964Chlorobenzene溶媒

反応条件

温度
125 °C

実験手順

Aluminum chloride (2.6 g, 19.92 mmol) was added to a solution of N-(2-bromophenyl)cinnamamide (1.0 g, 3.32 mmol) in chlorobenzene, and the resulting mixture was heated at 125° C. for 2 h. The reaction mixture was then cooled to 50° C. and treated with ice-cold water (25 mL) to provide a brown precipitate. The precipitate was collected by vacuum filtration and dried in vacuo, then triturated with EtOH to provide 8-bromoquinolin-2(1H)-one (0.5 g, 67% yield) as an off-white solid. m/z (ESI, +ve) 226.2 (M+H)+

後処理

  1. temperatureThe reaction mixture was then cooled to 50° C.
  2. customto provide a brown precipitate
  3. filtrationThe precipitate was collected by vacuum filtration
  4. customdried in vacuo
  5. customtriturated with EtOH

出典と根拠

ORDレコード
ord-70bde04703204b5fb871d7eb38a46c36
出典データセット
uspto-grants-2016_07
特許番号
US09394297B2

関連ノート

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