Carbamic acid, ethyl ester → HCID 53993899, compound
Reaction equation
[CH2:1]([O:3][C:4](=[O:6])[NH2:5])[CH3:2].[Cl:7][C:8]1[C:12]([Cl:13])=[N:11][C:10](=[C:14](Cl)Cl)[N:9]=1.[O:17]1CCOCC1>>[CH2:1]([O:3][C:4](=[O:6])[NH:5][C:14]([C:10]1[NH:11][C:12]([Cl:13])=[C:8]([Cl:7])[N:9]=1)=[O:17])[CH3:2]Participants
4
Procedure
A solution of 20 g (0.225 mol) of carbamic acid ethyl ester and 21.8 g (0.1 mol) of 4,5-dichloro-2-dichloromethylene-imidazole in 50 ml of dioxane was heated briefly to the boil (about 115° C.) After cooling, the product was precipitated with water, filtered off, washed with water and dried. 15 g (60% of theory) of N-(4,5-dichloroimidazol-2-oyl)-carbamic acid ethyl ester with a melting point of 208° C. (from acetonitrile) were obtained.
Workup
- temperatureAfter cooling
- customthe product was precipitated with water
- filtrationfiltered off
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-060706b0d9554f57b67806d206df8f96
- Source dataset
- uspto-grants-1979_12
- Patent number
- US04179277
Reaction notes
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