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Aluminum(III) Chloride → 7-Bromo-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

HRID 52445
ノート
印刷プレビュー

反応式

HRID 52445 の反応式
[Al+3].[Cl-].[Cl-].[Cl-].[CH3:5][C:6]([CH3:18])=[CH:7][C:8]([NH:10][C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([Br:17])[CH:12]=1)=[O:9]>C(Cl)Cl>[CH3:5][C:6]1([CH3:18])[C:16]2[C:11](=[CH:12][C:13]([Br:17])=[CH:14][CH:15]=2)[NH:10][C:8](=[O:9])[CH2:7]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6451240Aluminum(III) ChlorideHCID 19177475N-3,3-Dimethylacryloyl-3-bromoaniline2 回

生成物 1

HCID 199637077-Bromo-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

Into a 500 ml round-buttom flask was placed 13.52 g (101 mmol) of AlCl3 under nitrogen purge and kept at 0° C. Thereafter, 22.41 g of N-3,3-dimethylacryloyl-3-bromoaniline (Compound 17) in 350 ml CH2Cl2 was slowly added by syringe. The reaction mixture was stirred at 0° C. for 72 h, and thereafter slowly quenched with small chunks of ice-cubes and finally with water. The aqueous layer was washed with CH2Cl2 and the organic layer was dried over Na2SO4. The solvent was evaporated and the residue purified by recrystallization from EtOAc-hexane to give the title compound as off-white solids.

後処理

  1. customInto a 500 ml round-buttom flask was placed
  2. customkept at 0° C
  3. customslowly quenched with small chunks of ice-cubes and finally with water
  4. washThe aqueous layer was washed with CH2Cl2
  5. dry with materialthe organic layer was dried over Na2SO4
  6. customThe solvent was evaporated
  7. customthe residue purified by recrystallization from EtOAc-hexane

出典と根拠

ORDレコード
ord-1062b5d1f0f24b1f95b2e920563ab6f5
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05616712

反応ノート

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