Ethanol → HCID 70608902, 화합물

HRID 597285노트

반응식

HRID 597285 반응식
[OH-:1].[K+].C(C[C:6]1[C:14]2[O:13][CH:12]=[C:11]([C:15]3[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=3)[C:10]=2[CH:9]=[CH:8][CH:7]=1)#N.[CH2:22]([OH:24])[CH3:23]>>[F:21][C:18]1[CH:17]=[CH:16][C:15]([C:11]2[CH:10]=[C:9]3[CH:8]=[CH:7][CH:6]=[C:14]3[O:13][C:12]=2[CH2:23][C:22]([OH:1])=[O:24])=[CH:20][CH:19]=1

참가 물질

4

반응물 3

HCID 702EthanolHCID 14797Potassium HydroxideHCID 21447365HCID 21447365, 화합물

생성물 1

HCID 70608902HCID 70608902, 화합물

실험 절차

Potassium hydroxide (85%, 49 g.), 7-cyanomethyl-3-(4-fluorophenyl)benzofuran (48.8 g., 0.194 mole) and 95% ethanol (500 ml.) are mixed and heated at reflux temperature overnight under a nitrogen atmosphere. The mixture is then concentrated by evaporation in vacuo, diluted with water and extracted with diethyl ether. The aqueous phase is filtered, then acidified by the slow addition of hydrochloric acid. The solid is collected by filtration and recrystallized from aqueous ethanol (65%) with treatment with decolorizing charcoal, giving yellow crystals. Another recrystallization from an ethanol-petroleum ether mixture (about 5:1) gives yellow crystals of 3-(4 -fluorophenyl)-7-benzofuranacetic acid, m.p. 169°-170° C.

후처리

  1. temperatureheated
  2. temperatureat reflux temperature overnight under a nitrogen atmosphere
  3. concentrationThe mixture is then concentrated by evaporation in vacuo
  4. additiondiluted with water
  5. extractionextracted with diethyl ether
  6. filtrationThe aqueous phase is filtered
  7. additionacidified by the slow addition of hydrochloric acid
  8. filtrationThe solid is collected by filtration
  9. customrecrystallized from aqueous ethanol (65%) with treatment with decolorizing charcoal
  10. customgiving yellow crystals
  11. customAnother recrystallization from an ethanol-petroleum ether mixture (about 5:1)

출처 및 근거

ORD 기록
ord-9c4aa895c2104b278b5acc2273ecb3ed
출처 데이터셋
uspto-grants-1977_03
특허 번호
US04013692

반응 노트

불러오는 중…