Ammonia → HCID 14745921, compound
Reaction equation
[Cl:1]/[C:2](/[C:10]([O:12][CH2:13][CH3:14])=[O:11])=[C:3](\Cl)/[C:4]([O:6][CH2:7][CH3:8])=[O:5].[NH3:15]>CN(C)C=O.C(O)(=O)C>[NH2:15]/[C:3](/[C:4]([O:6][CH2:7][CH3:8])=[O:5])=[C:2](\[Cl:1])/[C:10]([O:12][CH2:13][CH3:14])=[O:11]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 120 °C
Procedure
48.2 g (0.2 mol) of diethyl dichloromaleate were dissolved in 80 ml of dimethylformamide and 2 ml of glacial acetic acid, and the mixture was warmed to 100° C. Ammonia gas was then passed in. During this operation, the temperature increased to about 120° C. After 30 minutes, the temperature dropped back to 100° C.; the reaction was then complete. The solvent was then removed by vacuum distillation. The residue was taken up in methylene chloride, and the solution was washed with water. The methylene chloride solution was evaporated in a rotary evaporator. 38.9 g (87.8% yield) of diethyl aminochloromaleate were obtained as a yellow oil which solidified on trituration to form needle-shaped crystals (m.p. 84° C.-86° C.).
Workup
- additionthe temperature dropped back to 100° C.
- customThe solvent was then removed by vacuum distillation
- washthe solution was washed with water
- customThe methylene chloride solution was evaporated in a rotary evaporator
Sources & evidence
- ORD record
- ord-f3c27063a6ca45aa9a450ee2c0274c80
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05101067
Reaction notes
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