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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855325Generated: October 27, 2026

4-Benzyl-2,6-dichloropyrimidine → 4-Benzyl-2-chloro-pyrimidine

https://huagongshe.com/reaction/1855325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyl-2,6-dichloropyrimidineHCID 46223071—
CatalystZincHCID 23994—
SolventAmmoniaHCID 222—
SolventEthyl AcetateHCID 8857—
Product4-Benzyl-2-chloro-pyrimidineHCID 18353331102.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

To an emulsion of 6-benzyl-2,4-dichloro-pyrimidine (239 mg, 1 mmol) in 25% aqueous ammonia solution (1 mL) was added after stirring for 10 min at 0° C. zinc powder (82 mg, 1.25 mmol). The reaction was stirred at 20° C. for 16 h. The yellow suspension was diluted with ethyl acetate an insoluble material was filtered off. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate and evaporated under reduced pressure to yield the crude title compound (210 mg, 92%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962834B2
Source datasetuspto-grants-2015_02
ORD IDord-c51372fc5ba742a7b6bf8c65b587339b
Source noteuspto-grants-2015_02