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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651419Generated: October 31, 2026

Formamide → HCID 135704063, compound

https://huagongshe.com/reaction/651419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantAmmonium AcetateHCID 517165—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 45156320HCID 45156320—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 135704063HCID 135704063—

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethyl-(3-trifluoromethylphenyl)acetoacetate (15.3 g, 0.056 mol) is added to a solution of ammonium acetate (21.6 g, 0.28 mol) in ethanol (100 ml) and the mixture is refluxed for 3 hours. The solution is concentrated under reduced pressure and then suspended in ethyl acetate. The suspension is washed with water and saturated brine and the organic layer concentrated. The material is then dissolved in dimethylsulfoxide (125 ml) and formamide (20 ml) and potassium tert-butoxide (1.28 g, 0.011 mol) are added. The solution is heated for 18 hours at 100° C. Upon cooling the solution is poured into ice (1000 ml) and glacial acetic acid (20 ml). The resulting solid is collected and air dried. The material is then triturated with diethyl ether and is air dried to give 6-(3-trifluoromethylbenzyl)pyrimidin-4-one (7.20 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281219B1
Source datasetuspto-grants-2001_08
ORD IDord-09366f1604d544b7ada76a226a4215ab
Source noteuspto-grants-2001_08