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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884547Generated: October 31, 2026

Benzoyl chloride → HCID 2785824, compound

https://huagongshe.com/reaction/1884547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantDimethylbarbituric acidHCID 69860—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 2785824HCID 278582464%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1,3-dimethylbarbituric acid (5 g, 32.02 mmol), 4-dimethylaminopyridine (4.74 g, 38.79 mmol) in dry CH2Cl2 (75 ml) was cooled to 0° C. and benzoyl chloride (4.95 g, 35.22 mmol) added dropwise in 15 min. The reaction mixture was stirred for 3 h at room temperature, diluted with CH2Cl2 (150 ml) and washed with 2 N HCl solution (40 ml). The organic phase was dried over MgSO4 and evaporated. The residue was crystallised from diisopropylether then recrystallised from MeOH, giving 5-benzoyl-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione 3 (5.32 g, 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06765089B1
Source datasetuspto-grants-2004_07
ORD IDord-2b42ef97718a48a0823b4de5c04dc5db
Source noteuspto-grants-2004_07