Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172587Generated: October 31, 2026

Potassium Carbonate → 3-[4-(4-methoxy-benzyloxy)-2-methyl-6-oxo-6H-pyrimidin-1-yl]-4-methyl-benzoic acid methyl ester

https://huagongshe.com/reaction/2172587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant3-(4-hydroxy-2-methyl-6-oxo-6H-pyrimidin-1-yl)-4-methyl-benzoic acid methyl esterHCID 136387805—
SolventDimethylformamideHCID 6228—
SolventEthylacetate heptaneHCID 21899848—
Product3-[4-(4-methoxy-benzyloxy)-2-methyl-6-oxo-6H-pyrimidin-1-yl]-4-methyl-benzoic acid methyl esterHCID 8668628222.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-(4-hydroxy-2-methyl-6-oxo-6H-pyrimidin-1-yl)-4-methyl-benzoic acid methyl ester from Step D (800 mg, 66% purity, 1.93 mmol) in N,N-dimethylformamide (3 mL) was added 4-methoxybenzyl chloride (0.26 mL, 1.93 mmol), potassium carbonate (666 mg, 4.82 mmol) and 18-crown-6 (80 mg). The slurry was heated at 60° C. for two hours. The solution was allowed to cool to ambient temperature and was partitioned between ethyl acetate and water. The organic layer was washed with water and brine and dried over magnesium sulfate. The slurry was filtered and concentrated to a brown oil. Normal phase chromatography (ethyl acetate/heptane) provided the alkylated product as a white solid (170 mg, 22% yield). MS (M+H): 395

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056110B2
Source datasetuspto-grants-2015_06
ORD IDord-b8bb6c2c86b14ecf878f5e179be5d513
Source noteuspto-grants-2015_06