Reaction #7320
ord-3a033b9a8a09491ca1a0fe7d07fca5cf
Reaction equation
Reagents
Conditions
Workup
- 1Otherreaction
- 2ConcentrationAfter concentration at 60° C./14 mmHg to a volume of ca. 500 mL
- 3workup.ADDITIONthe residue was diluted with acetone (500 mL)
- 4FiltrationThe resulting precipitate was collected by filtration
- 5Washwashed with acetone
- 6Otherdried by suction
- 7Otherat 50° C./25 mmHg to give crude 5-(hydroxymethyl)-1,3-dihydropyrimidine-2,4-dione (250 g) as a white solid
- 8ConcentrationThe combined mother liquor and washes were concentrated to a volume of ca. 100 mL
- 9FiltrationThe resulting precipitate was collected by filtration
- 10Washwashed with acetone
- 11Otherdried by suction
Procedure
A 2-L, three-necked flask equipped with a mechanical stirrer, thermometer, condenser, and nitrogen-inlet bubbler was charged with uracil (185.0 g, 1650 mmol) (Aldrich), paraformaldehyde (61.50 g, 2050 mmol as formaldehyde) (Aldrich), and a solution of potassium hydroxide (86.9%, 59.95 g, 928.5 mmol) (Aldrich) in water (1.445 L). The mixture was stirred at 50-52° C. for 68 h. TLC analysis indicated complete reaction. After concentration at 60° C./14 mmHg to a volume of ca. 500 mL, the residue was diluted with acetone (500 mL). The resulting precipitate was collected by filtration, washed with acetone, and dried by suction, then at 50° C./25 mmHg to give crude 5-(hydroxymethyl)-1,3-dihydropyrimidine-2,4-dione (250 g) as a white solid. The combined mother liquor and washes were concentrated to a volume of ca. 100 mL and a solution of hydroxylamine hydrochloride (27.52 g, 396.0 mmol, Aldrich) in water (100 mL) was added. The resulting precipitate was collected by filtration, washed with acetone, and dried by suction to give second crop of crude 5-(hydroxymethyl)-1,3-dihydropyrimidine-2,4-dione (34 g) as a white solid. The two lots were combined (244 g, 4% overweight) and used directly in the next step.