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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247082생성일: 2026년 10월 26일

Triethylamine → 1-(4-Chlorophenoxy)methyl-5-trifluoromethylpyrimidin-2-one

https://huagongshe.com/reaction/247082

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물alpha,4-DichloroanisoleHCID 88801—
반응물5-(Trifluoromethyl)pyrimidin-2(1H)-oneHCID 13317027—
용매DichloromethaneHCID 6344—
생성물1-(4-Chlorophenoxy)methyl-5-trifluoromethylpyrimidin-2-oneHCID 13317031—

반응 단계

A solution of 1-chloromethoxy-4-chloro-benzene [see Preparation 11] (0.35 mmol) in dichloromethane (1 ml) was added with stirring at room temperature to a solution prepared from 5-trifluoromethyl-pyrimidin-2-one (0.33 mmol) and triethylamine (0.33 mmol) in dichloromethane (5 ml). The mixture was stirred at room temperature for 24 h and then it was stirred at 70° C. for 30 min, the solvent was then distilled off, the residue triturated with water, the residual material extracted with chloroform and the dried (MgSO4) chloroform solution evaporated to yield the product, 60 mg (62%), as a mixture of the N- and O-isomers in the ratio 5:1. The isomers were separated by their different solubilities in ether, the O-isomer being the more soluble. The title compound, the N-isomer had m.p. 98° C. (Found C46.78; H2.88. Calc. for C12H8ClF3N2O3 : C47.30; H2.65)1H NMR (CDCl3): δ 5.85 (CH2), 6.8-7.4 (Ph), 8.15 (H-4, J4.6 3 Hz) 8.76 (H-6) MS [70 eV; m/z (% rel. int.)]; 177 (100), 150(10), 75(5), IR (KBr); 1690cm-1 (CO).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04705791
출처 데이터셋uspto-grants-1987_11
ORD IDord-e11945b33d024b56ad1a7d429e375eb8
출처 메모uspto-grants-1987_11