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

HRID 52445
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인쇄 미리보기

반응식

HRID 52445 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6451240Aluminum(III) ChlorideHCID 19177475N-3,3-Dimethylacryloyl-3-bromoaniline2회

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-1062b5d1f0f24b1f95b2e920563ab6f5
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05616712

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