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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357074Generated: October 26, 2026

1-Bromo-3-chloropropane → 3-benzyl-6-chloro-1-(3-chloropropyl)-5-phenylpyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/357074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant3-benzyl-6-chloro-5-phenylpyrimidine-2,4(1H,3H)-dioneHCID 15027509—
SolventDimethylformamideHCID 6228—
Product3-benzyl-6-chloro-1-(3-chloropropyl)-5-phenylpyrimidine-2,4(1H,3H)-dioneHCID 15027542—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 78.19 g (250 mmol) of 3-benzyl-6-chloro-5-phenylpyrimidine-2,4(1H,3H)-dione and 55.3 g (400 mmol) of potassium carbonate in 450 ml of N,N-dimethylformamide, 49.4 ml (500 mmol) of 1-bromo-3-chloropropane was added at room temperature. This mixture was stirred at 80° C. for 5 hours. After cooling, the reaction mixture was concentrated to dryness; the resulting residue was dissolved in chloroform-water. After the organic layer was washed with water and dried, the solvent was distilled off to yield an oily substance, which was then purified by column chromatography (eluent, n-hexane/ethyl acetate=5/1→2/1) to yield 71.89 g (73.9%, yellow oily substance) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840732
Source datasetuspto-grants-1998_11
ORD IDord-8cbc3eacec5e49abae9e5350591089e8
Source noteuspto-grants-1998_11