반응 #586122

ord-1d7942bb5aa14b6aa81d497c3f7748d6

반응 방정식

O
water
N#Cc1ccc(-c2ccc(C(F)(F)F)cc2)cc1S
2-mercapto-4-(4-trifluoromethylphenyl)benzonitrile
CC(C)(C)[O-].[K+]
potassium tert-butoxide
C=CCSc1cc(-c2ccc(C(F)(F)F)cc2)ccc1C#N
2-(2-propenylthio)-4-(4-trifluoromethylphenyl)benzonitrile
수율 43.5%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The resulting reaction mixture
  2. 2
    추출extracted with 50 ml of ethyl acetate twice
  3. 3
    세척The ethyl acetate layer was washed with 50 ml of water twice
  4. 4
    건조dried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONthe ethyl acetate was distilled off under reduced pressure
  6. 6
    기타Purification of the residue by silica gel column chromatography

실험 절차

1.0 g (3.6 mmol) of 2-mercapto-4-(4-trifluoromethylphenyl)benzonitrile, 0.45 g (4.0 mmol) of potassium tert-butoxide and 0.5 g (4.1 mmol) of 3-propenyl bromide were stirred in 20 ml of N,N-dimethylformamide at room temperature for 1 hour. The resulting reaction mixture was poured into 20 ml of water and extracted with 50 ml of ethyl acetate twice. The ethyl acetate layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 0.5 g of 2-(2-propenylthio)-4-(4-trifluoromethylphenyl)benzonitrile (yield 43.0%) as yellow crystals (m.p. 89-90° C.).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07767626B2uspto-grants-2010_08