Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458Generated: October 26, 2026

N-methyl-2-pyrrolidone → 3,6-diethyl-2-phenyl-5-trifluoromethyl-4(3H)-pyrimidinone

https://huagongshe.com/reaction/1458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium TrifluoroacetateHCID 517019—
Reactant3,6-diethyl-5-iodo-2-phenyl-4(3H)-pyrimidinoneHCID 19690660—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethyl EtherHCID 3283—
Product3,6-diethyl-2-phenyl-5-trifluoromethyl-4(3H)-pyrimidinoneHCID 1969072042.2%

Reaction Steps

A mixture of 1.00 g (2.8 mmol) of 3,6-diethyl-5-iodo-2-phenyl-4(3H)-pyrimidinone, 1.08 g (5.7 mmol) of copper (I) iodide, 1.54 g (11.3 mmol) of sodium trifluoroacetate and 8 mL of anhydrous N-methylpyrrolidinone was heated at 175 C for 2 h. The mixture was cooled, diluted with 175 mL of ether, washed with four 50 mL portions of water and dried over MgSO4. Removal of the solvent on the rotovap afforded 0.92 g of crude product as a brown oil. This material was purified by flash chromatography on a 25 g column of silica gel eluting with 100 mL portions of 0, 10, 20, 30, 40, 50 and 75% ether in hexanes to afford 0.35 g of 3,6-diethyl-2-phenyl-5-trifluoromethyl-4(3H)-pyrimidinone (compound 185) as a white solid. 1H-NMR (CDCl3) 1.25(3H,t), 1.30(3H,t), 2.8(2H,q), 4.0(2H,q), 7.5(5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726124
Source datasetuspto-grants-1998_03
ORD IDord-5d84c8f338a741eebe88ed5f50eec903
Source noteuspto-grants-1998_03