Reaction equation
[Cl:1][C:2]1=[C:3]([Cl:9])[C:4]([O:6][C:7]1=O)=[O:5].Cl.[CH3:11][NH2:12].C(O)(=O)C.C[O-].[Na+]>O>[Cl:1][C:2]1[C:7](=[O:6])[N:12]([CH3:11])[C:4](=[O:5])[C:3]=1[Cl:9]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 10 °C
Procedure
A 3L-three-necked flask fitted with a magnetic stir bar, digital thermocouple/thermometer, nitrogen purge and solid addition funnel was charged with 450 g (269.5 mol) of dichloromaleic anhydride, 191 g (282.8 mol) of methylamine hydrochloride and 1.6 L of acetic acid. The reaction mixture was then cooled to 10° C., and 160 g NaOMe added from the solid addition funnel over 1 hour while keeping the temperature between 10-12° C. The reaction mixture was allowed to stir at room temperature for 42 hours (24 hours is sufficient) then heated to 100° C. for 3 hours. HPLC analysis at this time indicated that all the starting material had disappeared. The reaction was cooled to room temperature and 2 L water was added. The mixture was then cooled to 3-10° C. for 1 hour and filtered at 4° C. The solids were then rinsed with 2 L of cold deionized water. The pale yellow solid dried in an air oven overnight to afford 360 g (75%) yield of the titled compound.
Workup
- customA 3L-three-necked flask fitted with a magnetic stir bar
- customdigital thermocouple/thermometer, nitrogen purge
- additionsolid addition funnel
- custombetween 10-12° C
- temperaturethen heated to 100° C. for 3 hours
- temperatureThe reaction was cooled to room temperature
- temperatureThe mixture was then cooled to 3-10° C. for 1 hour
- filtrationfiltered at 4° C
- washThe solids were then rinsed with 2 L
- customThe pale yellow solid dried in an air oven overnight
Sources & evidence
- ORD record
- ord-649fa3f6f2fe4238a9450b19fa5e0632
- Source dataset
- uspto-grants-1999_07
- Patent number
- US05919946
Linked notes
Loading…