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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1458Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1458

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-methyl-2-pyrrolidoneHCID 13387—
EduktSodium TrifluoroacetateHCID 517019—
Edukt3,6-diethyl-5-iodo-2-phenyl-4(3H)-pyrimidinoneHCID 19690660—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3,6-diethyl-2-phenyl-5-trifluoromethyl-4(3H)-pyrimidinoneHCID 1969072042,2%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726124
Quelldatensatzuspto-grants-1998_03
ORD IDord-5d84c8f338a741eebe88ed5f50eec903
Quellennotizuspto-grants-1998_03