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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106764Generated: October 25, 2026

Ethyl Bromide → 3-ethyl-1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/2106764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPotassium HydroxideHCID 14797—
Reactant1-(4-Nitrophenyl)pyrimidine-2,4-dioneHCID 11276338—
SolventDimethylacetamideHCID 31374—
Product3-ethyl-1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedioneHCID 1512547965.6%

Reaction Steps

A mixture of 3 parts of 1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione, 1,4 parts of potassium hydroxide and 67.5 parts of N,N-dimethylacetamide was stirred for 1 hour at room temperature under nitrogen atmosphere. 1.52 Parts of bromoethane were added and stirring was continued overnight at room temperature. The reaction mixture was poured into 100 parts of ice water. The product was filtered off and stirred in methanol. The product was filtered off and dried in vacuo at 60° C., yielding 2.4 parts (65.6%) of 3-ethyl-1-(4-nitro-phenyl)-2,4(1H,3H)-pyrimidinedione; mp. 182.5° C. (int. 24).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931444
Source datasetuspto-grants-1990_06
ORD IDord-d072a9a384e947f2a9bfee02dda21a87
Source noteuspto-grants-1990_06