Cesium carbonate → HCID 57633709, Verbindung

HRID 2109091Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2109091
[NH2:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]([F:13])([F:12])[F:11])[CH:3]=1.C(=O)([O-])[O-].[Cs+].[Cs+].Br[CH2:21][CH2:22][F:23]>C(#N)C>[F:23][CH2:22][CH2:21][NH:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]([F:11])([F:12])[F:13])[CH:3]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

To a solution of 4-amino-2-(trifluoromethyl)benzonitrile (0.100 g, 0.54 mmol) in acetonitrile (3 mL) was added cesium carbonate (0.438 g, 1.34 mmol) and 1-bromo-2-fluoroethane (0.340 g, 2.68 mmol). The mixture was heated in a microwave at 120° C. for 15 min. Upon cooling, additional 1-bromo-2-fluoroethane (0.340 g, 2.68 mmol) was added and the reaction was heated in the microwave at 140° C. for 20 min. Upon cooling, the solids were filtered off and washed with ethyl acetate. The filtrate was concentrated in vacuo and the residue was purified by radial chromatography (10-40% ethyl acetate-hexane gradient) to give 0.100 g of a mixture (6:1) of the title compound and 4-[bis(2-fluoroethyl)amino]-2-(trifluoromethyl)benzonitrile as a white solid, which was used as such in the next reaction.

Aufarbeitung

  1. temperatureUpon cooling
  2. temperaturethe reaction was heated in the microwave at 140° C. for 20 min
  3. temperatureUpon cooling
  4. filtrationthe solids were filtered off
  5. washwashed with ethyl acetate
  6. concentrationThe filtrate was concentrated in vacuo
  7. customthe residue was purified by radial chromatography (10-40% ethyl acetate-hexane gradient)

Quellen und Nachweise

ORD-Eintrag
ord-32bfd6bb643b4fa7b42884e7c154abd5
Quelldatensatz
uspto-grants-2009_04
Patentnummer
US07514470B2

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