Reaction #1540

ord-2b0378d7412b4bedb3ed0ed2242b2a38

Reaction equation

Cl.N=C(N)c1ccccc1.O
benzamidine hydrochloride hydrate
CC(=O)[O-].[Na+]
sodium acetate
CCOC(=O)C=C(OCC)OCC
ethyl 3,3-diethoxyacrylate
CS(C)=O
DMSO
CCOc1cc(=O)[nH]c(-c2ccccc2)n1
6-ethoxy-2-phenyl-4(3H)-pyrimidinone
Yield 57.0%

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 1 H-NMR (d6-DMSO) δ 1.35(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: US05726124uspto-grants-1998_03