Carbon Tetrachloride → HCID 178526513, Verbindung

HRID 2370965

Reaktionsgleichung

Reaktionsgleichung von HRID 2370965
[C:1]([C:5](O)=O)([F:4])([F:3])[F:2].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CCN(CC)CC.[CH:34]1([C:37]2[CH:42]=[CH:41][C:40]([N+:43]([O-:45])=[O:44])=[CH:39][C:38]=2[NH2:46])[CH2:36][CH2:35]1.C(Cl)(Cl)(Cl)[Cl:48]>>[Cl:48]/[C:5](=[N:46]\[C:38]1[CH:39]=[C:40]([N+:43]([O-:45])=[O:44])[CH:41]=[CH:42][C:37]=1[CH:34]1[CH2:36][CH2:35]1)/[C:1]([F:4])([F:3])[F:2]

Komponenten

6

Edukt 5

HCID 5943Carbon TetrachlorideHCID 6422Trifluoroacetic acidHCID 8471TriethylamineHCID 11776TriphenylphosphineHCID 580658012-Cyclopropyl 5-nitrobenzenamine

Produkt 1

HCID 178526513HCID 178526513, Verbindung

Versuchsvorschrift

A mixture of CF3CO2H (0.98 mL, 12.65 mmol, 0.9 eq), PPh3 (9.21 g, 35.13 mmol, 2.5 eq) and Et3N (1.96 mL, 14.05 mmol, 1.0 eq), in 25 mL CCl4 was stirred at 0° C. for 10 minutes. 2-cyclopropyl-5-nitrobenzeneamine (2.50 g, 14.05 mmol, 1.0 eq) was then added to the reaction mixture and the mixture was heated to reflux for 12 hours. Solvent was removed under reduced pressure and the residue was purified by column chromatography, eluting with n-hexane:ethyl acetate (10:1), giving the (Z)—N-(1-chloro-2,2,2-trifluoroethylidene)-2-cyclopropyl-5-nitrobenzenamine intermediate in semi pure form as a light yellow solid. This compound was taken to the next step with out further purification.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 12 hours
  3. customSolvent was removed under reduced pressure
  4. customthe residue was purified by column chromatography
  5. washeluting with n-hexane:ethyl acetate (10:1)

Quellen und Nachweise

ORD-Eintrag
ord-66938c57ffc94ddd9dcb15c0d2be5faa
Quelldatensatz
uspto-grants-2014_04
Patentnummer
US08710223B2

Verknüpfte Notizen

Wird geladen…