Reaction #1550416
ord-17711c91b7784461abcde2829759fd38
Reaction equation
Reagents
None
Solvents
Conditions
Temperature
120°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1TemperatureThe mixture was cooled
- 2Washwashed with two 100 mL portions of ether
- 3Filtrationthe precipitate was collected by filtration
- 4Otherdried under vacuum at 50° C.
Procedure
A mixture of 3.14 g (20.0 mmol) of benzamidine hydrochloride hydrate, 1.65 g (20.1 mmol) of powdered anhydrous sodium acetate, 4.17 g (22.2 mmol) of ethyl 3,3-diethoxyacrylate and 10 mL of DMSO was heated at 120° C. for 8 h. The mixture was cooled, diluted with 50 mL of 5% aqueous NaOH and washed with two 100 mL portions of ether. The aqueous layer was acidified with concentrated hydrochloric acid and the precipitate was collected by filtration and dried under vacuum at 50° C. to furnish 2.28 g (57%) of crude 6-ethoxy-2-phenyl-4(3H)-pyrimidinone as a yellow solid 1H-NMR (d6-DMSO) δ1.35(3H,t), 4.33(2H,q), 5.60(1H,s), 7.50(3H,m), 8.2(2H,m).