Hydrochloric Acid → 4-(3-Bromo-4-methoxy-phenyl)-4-methyl-3-oxo-pentanoic acid ethyl ester

HRID 61811

반응식

HRID 61811 반응식
CS(O)(=O)=[O:3].[Br:6][C:7]1[CH:8]=[C:9]([C:15]([CH3:19])([CH3:18])[C:16]#N)[CH:10]=[CH:11][C:12]=1[O:13][CH3:14].[C:20]([O:23][CH2:24][CH2:25]Br)(=[O:22])[CH3:21].Cl>[Zn].C1COCC1>[CH2:24]([O:23][C:20](=[O:22])[CH2:21][C:16](=[O:3])[C:15]([C:9]1[CH:10]=[CH:11][C:12]([O:13][CH3:14])=[C:7]([Br:6])[CH:8]=1)([CH3:19])[CH3:18])[CH3:25]

참가 물질

7

반응 조건

온도
80 °C

실험 절차

To the THF suspension of zinc (5.72 g, 2 eq.), methanesulfonic acid (25.6 μl, 0.01 eq.) was added, and then stirred at 80° C. for 10 min. Then, the THF solution of 2-(3-bromo-4-methoxy-phenyl)-2-methyl-propionitrile (10 g, 39.35 mmol) was added, followed by addition of bromoethyl acetate (11.07 ml, 1.6 eq.) over 1 hr. The mixture was further stirred for 30 min. To the reaction solution, 4 M hydrochloric acid was added, and stirred at room temperature overnight. After extraction with ethyl acetate, the organic layer was washed with brine and dried over sodium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (orange oily substance, 9.74 g, 72%).

후처리

  1. additionwas added
  2. stirringThe mixture was further stirred for 30 min
  3. stirringstirred at room temperature overnight
  4. extractionAfter extraction with ethyl acetate
  5. washthe organic layer was washed with brine
  6. dry with materialdried over sodium sulfate
  7. customThe drying agent was removed by filtration
  8. customthe residues obtained
  9. concentrationafter concentration under reduced pressure
  10. customwere purified by silica gel column chromatography (ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-e3caf457cc424c3a82933351d7c7f175
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09440922B2

연결된 노트

불러오는 중…