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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1982566생성일: 2026년 10월 27일

5-Chloropyrimidin-2-ol hydrochloride → 1-(3-Trifluoromethylphenoxy)methyl-5-chloropyrimidin-2-one

https://huagongshe.com/reaction/1982566

반응식

참여 물질

역할이름HCID투입량
반응물5-Chloropyrimidin-2-ol hydrochlorideHCID 12648523—
반응물1-(Chloromethoxy)-3-(trifluoromethyl)benzeneHCID 13097733—
용매DichloromethaneHCID 6344—
생성물1-(3-Trifluoromethylphenoxy)methyl-5-chloropyrimidin-2-oneHCID 20161332—

반응 단계

A solution of 1-chloromethoxy-3-trifluoromethylbenzene [see Preparation 4) (7 mmol) in dichloromethane (10 ml) was added to a solution of 5-chloropyrimidin-2-one hydrochloride (70 mmol) in dichloromethane (30 ml) and the mixture stirred at room temperature for 18 h. The solvent was then distilled off, the mixture triturated with water, the residual solid extracted with chloroform and the dried (MgSO4) chloroform solution evaporated; yield 1.88 g (94%). The product was a mixture of the N- and O-isomer in the ratio 3:1. The isomers were separated by the difference in their solutilities in tetrachloromethane, the O-isomer being the more solunble. The title compound, the N-isomer was isolated in a non-crystalline form. 1H NMR (CDCl3) δ 5.82 (CH2), 7.1-7.3 (Ph), 7.85 (H-4, J4,6 3 Hz), 8.45 (H-6).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04596870
출처 데이터셋uspto-grants-1986_06
ORD IDord-73bcde404abf44a5b99a87f2a87d64a9
출처 메모uspto-grants-1986_06