戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 247082作成日:2026年10月27日

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

https://huagongshe.com/reaction/247082

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物alpha,4-DichloroanisoleHCID 88801—
反応物5-(Trifluoromethyl)pyrimidin-2(1H)-oneHCID 13317027—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Chlorophenoxy)methyl-5-trifluoromethylpyrimidin-2-oneHCID 13317031—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04705791
出典データセットuspto-grants-1987_11
ORD IDord-e11945b33d024b56ad1a7d429e375eb8
出典メモuspto-grants-1987_11