Dimethylformamide → Ethyl[(6,7-dichloro-2-acetylbenzo[b]thien-5-yl)oxy]acetate

HRID 370984노트

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HRID 370984 반응식
[C:1]([C:4]1[S:8][C:7]2[C:9]([Cl:15])=[C:10]([Cl:14])[C:11]([OH:13])=[CH:12][C:6]=2[CH:5]=1)(=[O:3])[CH3:2].Br[CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19].C(=O)([O-])[O-].[K+].[K+].CN(C)C=O>CC(=O)CC>[CH2:21]([O:20][C:18](=[O:19])[CH2:17][O:13][C:11]1[C:10]([Cl:14])=[C:9]([Cl:15])[C:7]2[S:8][C:4]([C:1](=[O:3])[CH3:2])=[CH:5][C:6]=2[CH:12]=1)[CH3:22]

참가 물질

6

실험 절차

To a solution of 9.0 g of 2-acetyl-6,7-dichloro-5-hydroxybenzo[b]thiophene and 200 ml of 2-butanone is added a solution of 6.62 g of ethyl bromoacetate in 50 ml of 2-butanone, 5.2 g of potassium carbonate and 2.2 ml of dimethylformamide. The reaction mixture is heated under reflux for 2 hrs, allowed to cool and filtered. The filtrate is extracted with ether (3 times). The layers are separated and the organic phase is washed with water, saturated sodium chloride solution, dried and filtered. The filtrate is evaporated. The residue is dissolved in dichloromethane and chromatographed on alumina, using dichloromethane as the eluant. Evaporation of the eluant gives 5.1 g of ethyl[(6,7-dichloro-2-acetylbenzo[b]thien-5-yl)oxy]acetate.

후처리

  1. temperatureThe reaction mixture is heated
  2. temperatureunder reflux for 2 hrs
  3. temperatureto cool
  4. filtrationfiltered
  5. extractionThe filtrate is extracted with ether (3 times)
  6. customThe layers are separated
  7. washthe organic phase is washed with water, saturated sodium chloride solution
  8. customdried
  9. filtrationfiltered
  10. customThe filtrate is evaporated
  11. dissolutionThe residue is dissolved in dichloromethane
  12. customchromatographed on alumina
  13. customEvaporation of the eluant

출처 및 근거

ORD 기록
ord-0bf20c0f6a074e1d873e012dd1a2c661
출처 데이터셋
uspto-grants-1985_07
특허 번호
US04528399

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