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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451Generated: October 25, 2026

Sodium Hydroxide → 6-carboxy-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone

https://huagongshe.com/reaction/1451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant6-ethoxycarbonyl-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 19690722—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product6-carboxy-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 1969071553.2%

Reaction Steps

To a solution of 1.81 g (6.1 mmol) of 6-ethoxycarbonyl-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone in 100 mL of ethanol and 50 mL of THF was added 50 mL of 5% aqueous sodium hydroxide. The mixture was stirred at room temperature for 24 h and rotovapped to remove the bulk of the organic solvents. The residue was diluted with 50 mL of 5% aqueous sodium hydroxide and washed with 100 mL of ether. The aqueous phase was acidified with concentrated hydrochloric acid and extracted with two 100 mL portions of ethyl acetate. The combined ethyl acetate extracts were washed with 50 mL of brine, dried over MgSO4 and concentrated to leave 0.87 g (53%) of crude 6-carboxy-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726124
Source datasetuspto-grants-1998_03
ORD IDord-c70bc697c73a4481b3467e71a66893b5
Source noteuspto-grants-1998_03