Ethanol → HCID 70608902, Verbindung

HRID 597285Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 597285
[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

Komponenten

4

Versuchsvorschrift

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.

Aufarbeitung

  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)

Quellen und Nachweise

ORD-Eintrag
ord-9c4aa895c2104b278b5acc2273ecb3ed
Quelldatensatz
uspto-grants-1977_03
Patentnummer
US04013692

Notizen zur Reaktion

Wird geladen…