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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075295Generated: October 31, 2026

Ethyl 4-chloroacetoacetate → S-[(3,4-Dihydro-2-(1-methylethyl)-4-oxo-6-pyrimidinyl)methyl] O,O-dimethyl phosphorodithioate

https://huagongshe.com/reaction/1075295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloroacetoacetateHCID 69484—
Reactant2-MethylpropanimidamideHCID 415118—
ReactantAmmonium O,O-dimethyl dithiophosphateHCID 6451175—
ReactantHCID 178440240HCID 178440240—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductS-[(3,4-Dihydro-2-(1-methylethyl)-4-oxo-6-pyrimidinyl)methyl] O,O-dimethyl phosphorodithioateHCID 135665134—

Reaction Steps

The intermediate, 6-(chloromethyl)-2-(1-methylethyl)-4(1H)pyrimidinone, was prepared according to Swiss patent 524617 from ethyl 4-chloroacetoacetate and isobutyramidine. m.p. 123°-125°. The intermediate chloromethyl compound (25 g) was stirred with 50 ml methanol at room temperature. To this mixture was added, dropwise, a solution of 25 g ammonium dimethyl phosphorodithioate dissolved in 500 ml methanol. The mixture was then heated to reflux for 6 hours, then the solvent was evaporated under reduced pressure yielding a solid. The solid was dissolved in dichloromethane and washed with water, separated, dried, and the solvent was evaporated. The remaining solid was recrystallized from toluene; yield: 15.9 g, m.p. 89°-93°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04395551
Source datasetuspto-grants-1983_07
ORD IDord-921e6e77ba944dc38469bfcabd59faa0
Source noteuspto-grants-1983_07