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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12673Generated: October 26, 2026

Water → 3-Benzoyl-1-(3-chloro-propyl)-5-iodo-1H-pyrimidine-2,4-dione

https://huagongshe.com/reaction/12673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPropane, bromochloro-HCID 36872—
Reactant3-Benzoyl-5-iodo-1H-pyrimidine-2,4-dioneHCID 11163664—
SolventDimethylformamideHCID 6228—
Product3-Benzoyl-1-(3-chloro-propyl)-5-iodo-1H-pyrimidine-2,4-dioneHCID 5933759298.1%

Reaction Steps

3-Benzoyl-5-iodo-1H-pyrimidine-2,4-dione (Prep36, 3 g, 8.77 mmol) and K2CO3 (1.2 g, 8.77 mmol) were suspended in dry DMF (45 mL) and stirred at room temperature for 1 h. Then, bromo-chloro-propane (2.7 mL, 17.5 mmol) was added dropwise and the mixture stirred at room temperature overnight. Water was added and the mixture was extracted with ethyl acetate. The organic phase was dried (Na2SO4), filtered and evaporated to give the title compound as a pale yellow oil (3.6 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727988B2
Source datasetuspto-grants-2010_06
ORD IDord-e06524fe40ad4c5a873fc85d108fc91f
Source noteuspto-grants-2010_06