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ETHYL 6-METHYL-2-OXO-4-PHENYL-1,2-DIHYDRO-5-PYRIMIDINECARBOXYLATE synthesis

6synthesis methods
-

Yield:69207-36-9 81%

Reaction Conditions:

with 1,4-bis(triphenylphosphonium)-2-butene peroxodisulfate in water;acetonitrile; for 4 h;Reflux;

Steps:

One-pot synthesis of pyrimidin-2(1H)-ones (general procedure).

General procedure: To a solution of ethyl acetoacetate(1 mmol), urea (1 mmol) and aromatic aldehyde (1 mmol) in acetonitrile-water (10 : 2 mL) was added 1,4-bis(triphenylphosphonium)-2-butene peroxodisulfate(1.1 mmol). The reaction mixture was refluxed upon stirring for 4 h. Water (10 mL) was added and the mixture was extracted with chloroform (3 × 15 mL). The organic layer was separated and dried overMgSO4. The solvent was evaporated and the product was purified by column chromatography on silica gelusing a mixture of ethyl acetate and n-hexane (1 : 3) asan eluent.

References:

Gorjizadeh;Afshari [Russian Journal of General Chemistry,2017,vol. 87,# 4,p. 842 - 845][Zh. Obshch. Khim.,2017,vol. 87,# 4,p. 842 - 845,4]