Hydrochloric Acid → 4-Amino-6-(2,4-dichlorophenyl)pyrimidine-2(1H)-thione

HRID 2389733

Reaktionsgleichung

Reaktionsgleichung von HRID 2389733
[Na].[NH2:2][C:3]([NH2:5])=[S:4].C([O-])C.[Na+].N[C:11]([C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=1[Cl:22])=[CH:12][C:13]#[N:14].Cl>C(O)C.O>[NH2:14][C:13]1[CH:12]=[C:11]([C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=2[Cl:22])[NH:5][C:3](=[S:4])[N:2]=1

Komponenten

8

Edukt 5

HCID 313Hydrochloric AcidHCID 2723790ThioureaHCID 2723922Sodium ethoxideHCID 5360545SodiumHCID 669113223-Amino-3-(2,4-dichlorophenyl)acrylonitrile

Produkt 1

HCID 583059934-Amino-6-(2,4-dichlorophenyl)pyrimidine-2(1H)-thione

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

16.51 g (718.08 mmol) of sodium are dissolved in 353 ml of ethanol, and 40.996 g (538.56 mmol) of thiourea are added to the sodium ethanolate solution prepared in this way, followed by 76.5 g (359.04 mmol) of 3-amino-3-(2,4-dichlorophenyl)acrylonitrile. The mixture is heated under reflux for 18 h and, after cooling, 500 ml of water are added. The mixture is neutralized with 1M hydrochloric acid, and the precipitate which has separated out is filtered off with suction. The latter is washed with water, suspended in THF and again filtered off with suction. It is washed with 300 ml of petroleum ether and then dried under high vacuum. 67.5 g (55% of theory) of the product are obtained as a solid.

Aufarbeitung

  1. customprepared in this way
  2. temperatureThe mixture is heated
  3. temperatureunder reflux for 18 h
  4. temperatureafter cooling
  5. customthe precipitate which has separated out
  6. filtrationis filtered off with suction
  7. washThe latter is washed with water
  8. filtrationagain filtered off with suction
  9. washIt is washed with 300 ml of petroleum ether
  10. customdried under high vacuum
  11. custom67.5 g (55% of theory) of the product are obtained as a solid

Quellen und Nachweise

ORD-Eintrag
ord-3c86153c3d3f4ce798dc081fdc1e4033
Quelldatensatz
uspto-grants-2012_09
Patentnummer
US08273752B2

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