Reaction #336834
ord-ca2f51cef2204ff4b0fd222f9034322c
Reaction equation
Reactants
Reagents
Conditions
Workup
- 1Otherremained at 25-30° C.
- 2TemperatureThe orange solution was heated to 50° C. over 30 minutes
- 3TemperatureThe reaction mixture was cooled to 30° C.
- 4Concentrationconcentrated to half volume at reduced pressure at 35-40° C.
- 5Other(resulting in foaming) over 30 minutes at 25-30° C. until the pH was about 1-2
- 6Othercrystallization of the product
- 7TemperatureAfter the mixture was cooled to 0° C. the solid
- 8Filtrationwas collected by filtration
- 9WashThe solid washed with water (3×60 mL)
- 10Othersuction-dried
- 11Otherdried in a vacuum-oven at 70° C.
Procedure
To a mixture of diethyl oxalacetate sodium salt (210 g, 950 mmol) in methanol (500 mL) and water (400 mL) was added 50% aqueous sodium hydroxide (80 g, 1.0 mol) in water (60 mL) over 30 minutes, over which time the temperature remained at 25-30° C. and the pH at 11-12. Then the stirred mixture was heated for an additional 30 min at 30° C. To this mixture was added cyclopropanecarboximidamide monohydrochloride (110 g, 910 mol). The orange solution was heated to 50° C. over 30 minutes and held at that temperature for 5 h. The reaction mixture was cooled to 30° C. and concentrated to half volume at reduced pressure at 35-40° C. and concentrated hydrochloric acid (140 g, 1.4 mol) was added gradually (resulting in foaming) over 30 minutes at 25-30° C. until the pH was about 1-2. The mixture was stirred at 5° C. for 1 h to complete crystallization of the product. After the mixture was cooled to 0° C. the solid was collected by filtration. The solid washed with water (3×60 mL), suction-dried, and then dried in a vacuum-oven at 70° C. to afford the title compound as a beige solid (100 g); m.p. 235-236° C. (dec.).