1,2-Dichloroethane → N-dimethylaminomethyleneguanine

HRID 274321Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 274321
[CH3:1][N:2]([CH3:5])[CH:3]=O.S(Cl)(Cl)=O.ClCCCl.[NH:14]1[C:23](=[O:24])[C:22]2[NH:21][CH:20]=[N:19][C:18]=2[N:17]=[C:15]1[NH2:16]>O>[CH3:1][N:2]([CH:5]=[N:16][C:15]1[NH:14][C:23](=[O:24])[C:22]2[NH:21][CH:20]=[N:19][C:18]=2[N:17]=1)[CH3:3]

Komponenten

6

Edukt 4

HCID 111,2-DichloroethaneHCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 135398634Guanine

Produkt 1

HCID 136087653N-dimethylaminomethyleneguanineAusbeute 85 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

131.6 g (1.8 mol) of N,N-dimethylformamide and 42.8 g (0.36 mol) of thionyl chloride were added to 500 ml of 1,2-dichloroethane, and then 45.3 g (0.3 mol) of guanine (manufactured by Sumika Fine Chemicals Co., Ltd.) was added, followed by stirring at 80° C. for 6 hours. After cooling, the reaction mixture was added to 1000 ml of water to separate out the water layer, and then the water layer was neutralized with sodium hydrogen carbonate. The precipitating crystal was collected by filtration and washed with 100 ml of water to yield 52.6 g (0.255 mol) of a white crystal of N-dimethylaminomethyleneguanine (yield 85%).

Aufarbeitung

  1. temperatureAfter cooling
  2. customto separate out the water layer
  3. filtrationThe precipitating crystal was collected by filtration
  4. washwashed with 100 ml of water

Quellen und Nachweise

ORD-Eintrag
ord-ecdf72925d834464a9b0943d991cf0b9
Quelldatensatz
uspto-grants-1995_02
Patentnummer
US05389637

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