3,4-Dichloroaniline → HCID 21923095, Verbindung

HRID 1965941Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1965941
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[Cl:9])[NH2:5].Cl[C:11]1[N:16]=[C:15]([Cl:17])[C:14]([C:18]([F:21])([F:20])[F:19])=[CH:13][N:12]=1.C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1>[Cl:1][C:2]1[CH:3]=[C:4]([NH:5][C:11]2[N:16]=[C:15]([Cl:17])[C:14]([C:18]([F:20])([F:21])[F:19])=[CH:13][N:12]=2)[CH:6]=[CH:7][C:8]=1[Cl:9]

Komponenten

5

Versuchsvorschrift

4.86 g of 3,4-dichloroaniline dissolved in 10 ml of dioxane are added to 6.51 g of 2,4-dichloro-5-trifluoromethyl-pyrimidine in 40 ml of dioxane at ambient temperature. Then 6 ml of 5 M potassium carbonate solution are added and the mixture is stirred for three days at ambient temperature. It is then filtered through Alox B (20 ml) and washed with dioxane. The filtrate is concentrated by evaporation, the residue dissolved in 50 ml methylene chloride and this solution is cooled in a bath of dry ice and acetone. The precipitate is suction filtered and the filtrate is cooled again. After suction filtering again the precipitates are combined and the filtrate is concentrated by evaporation. The residue is separated by chromatography through an RP18 column (gradient: acetonitrile: H2O=20:80 to 80:20).

Aufarbeitung

  1. filtrationIt is then filtered through Alox B (20 ml)
  2. washwashed with dioxane
  3. concentrationThe filtrate is concentrated by evaporation
  4. dissolutionthe residue dissolved in 50 ml methylene chloride
  5. temperaturethis solution is cooled in a bath of dry ice and acetone
  6. filtrationfiltered
  7. temperaturethe filtrate is cooled again
  8. filtrationAfter suction filtering again the precipitates
  9. concentrationthe filtrate is concentrated by evaporation
  10. customThe residue is separated by chromatography through an RP18 column (gradient: acetonitrile: H2O=20:80 to 80:20)

Quellen und Nachweise

ORD-Eintrag
ord-59b9740d392b4b75a61d33711ed6c912
Quelldatensatz
uspto-grants-2013_04
Patentnummer
US08420630B2

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