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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1982569Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1982569

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Eduktalpha,4-DichloroanisoleHCID 88801—
Edukt5-(Trifluoromethyl)pyrimidin-2(1H)-oneHCID 13317027—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(4-Chlorophenoxy)methyl-5-trifluoromethylpyrimidin-2-oneHCID 13317031—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04596870
Quelldatensatzuspto-grants-1986_06
ORD IDord-9ac24d7d4140418d98f704f9d76d6e56
Quellennotizuspto-grants-1986_06