Reaction #1550416

ord-17711c91b7784461abcde2829759fd38

Solvents

Conditions

Temperature
120°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureThe mixture was cooled
  2. 2
    Washwashed with two 100 mL portions of ether
  3. 3
    Filtrationthe precipitate was collected by filtration
  4. 4
    Otherdried 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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05300477uspto-grants-1994_04