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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1982569생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1982569

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); 1690 cm-1 (CO).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04596870
출처 데이터셋uspto-grants-1986_06
ORD IDord-9ac24d7d4140418d98f704f9d76d6e56
출처 메모uspto-grants-1986_06