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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1458생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1458

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물Sodium TrifluoroacetateHCID 517019—
반응물3,6-diethyl-5-iodo-2-phenyl-4(3H)-pyrimidinoneHCID 19690660—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Diethyl EtherHCID 3283—
생성물3,6-diethyl-2-phenyl-5-trifluoromethyl-4(3H)-pyrimidinoneHCID 1969072042.2%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726124
출처 데이터셋uspto-grants-1998_03
ORD IDord-5d84c8f338a741eebe88ed5f50eec903
출처 메모uspto-grants-1998_03