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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719241Generated: October 27, 2026

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

https://huagongshe.com/reaction/1719241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloropyrimidin-2-ol hydrochlorideHCID 12648523—
Reactant1-((Chloromethoxy)methyl)-3-(trifluoromethyl)benzeneHCID 13140584—
Product1-(3-Trifluoromethylbenzyloxy)methyl-5-chloropyrimidin-2-oneHCID 15650494—

Reaction Steps

was prepared as described in Example 3 from chloromethyl 3-trifluoromethyl-benzyl ether (see Preparation 6a and 6b) (10 mmol) and 5-chloropyrimidin-2-one hydrochloride (10 mmol) in 52%. (1.66 g) yield, m.p. 95° C. 1H NMR (CDCl3): δ4.77 (CH2Ph), 5.42 (CH2O), 7.3-7.7 (Ph), 7.82 and 8.55 (H-4, H-6, J 4 Hz). IR(KBr): 1660 cm-1 (CO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539324
Source datasetuspto-grants-1985_09
ORD IDord-0a7893dac825424a8848780db6244df1
Source noteuspto-grants-1985_09