Hydrochloric Acid → (4-Difluoromethoxyphenyl)(cyclopropyl) ketone

HRID 1388947

Reaktionsgleichung

Reaktionsgleichung von HRID 1388947
[Mg].[CH:2]1(Br)[CH2:4][CH2:3]1.[F:6][CH:7]([F:17])[O:8][C:9]1[CH:16]=[CH:15][C:12]([C:13]#N)=[CH:11][CH:10]=1.Cl.C([O:21]CC)C>O1CCCC1>[F:6][CH:7]([F:17])[O:8][C:9]1[CH:16]=[CH:15][C:12]([C:13]([CH:2]2[CH2:4][CH2:3]2)=[O:21])=[CH:11][CH:10]=1

Komponenten

7

Edukt 5

HCID 313Hydrochloric AcidHCID 3283Diethyl Ether2×HCID 78037BromocyclopropaneHCID 27369904-(Difluoromethoxy)benzonitrileHCID 5462224Magnesium

Produkt 1

HCID 20469192(4-Difluoromethoxyphenyl)(cyclopropyl) ketone

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

Upon a dry argon atmosphere, a mixture of 1.6 g (0.066 mole) of magnesium, 7.9 g (0.066 mole) of cyclopropylbromide, 60 ml of anhydrous diethyl ether, and 60 ml of anhydrous tetrahydrofuran was heated at reflux for 2.5 hours. The stirred mixture was cooled to room temperature, and a solution of 11.1 g (0.066 mole) of (4-difluoromethoxybenzonitrile) in 40 ml of anhydrous diethyl ether and 40 ml of anhydrous tetrahydrofuran was added during one hour. After complete addition, the mixture was heated at reflux for two hours, then stirred at room temperature for approximately 18 hours. A 100 ml portion of 2 N hydrochloric acid was added slowly to the mixture, and the whole was stirred for one hour. The mixture was extracted with three 100 ml portions of diethyl ether. The ether extracts were combined, dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to give an oil. The oil was subjected to column chromatography on silica gel, eluting with toluene/ethyl acetate (95:5), to give 8.3 g of (4-difluoromethoxyphenyl)(cyclopropyl) ketone.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureat reflux for 2.5 hours
  3. additionAfter complete addition
  4. temperaturethe mixture was heated
  5. temperatureat reflux for two hours
  6. stirringthe whole was stirred for one hour
  7. extractionThe mixture was extracted with three 100 ml portions of diethyl ether
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. customThe filtrate was evaporated under reduced pressure
  11. customto give an oil
  12. washeluting with toluene/ethyl acetate (95:5)

Quellen und Nachweise

ORD-Eintrag
ord-caeb65ea2cd242219019afdfdc16f935
Quelldatensatz
uspto-grants-1984_02
Patentnummer
US04434182

Verknüpfte Notizen

Wird geladen…