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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592258Generated: October 25, 2026

Water → 4-Chloro-6-(2,3-difluorobenzyl)pyrimidine

https://huagongshe.com/reaction/1592258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4,6-DichloropyrimidineHCID 70943—
Reactant1-(Bromomethyl)-2,3-difluoro-benzeneHCID 517984—
ReactantTmsciHCID 131723440—
Catalyst1,1-DibromoethaneHCID 11201—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-6-(2,3-difluorobenzyl)pyrimidineHCID 2259975238.4%

Reaction Steps

In 10 ml of tetrahydrofuran was suspended 1.3 g of zinc (powder), to which dibromoethane (2 drops) was added. The mixture was heated under reflux for 5 minutes, to which trimethylsilane chloride was added. The mixture was further heated under reflux for 5 minutes, to which a solution of 2.1 g of 2,3-difluorobenzyl bromide dissolved in 20 ml of tetrahydrofuran was slowly added with heating under reflux, followed by stirring for 20 minutes. (The solution thus obtained is referred to as solution G). In 10 ml of tetrahydrofuran were suspended 1.5 g of 4,6-dichloropyrimidine and 0.1 g of dichlorobistriphenylphosphine palladium, to which the above solution G was added, followed by heating under reflux for 3 hours and further stirring at room temperature for 12 hours. The reaction mixture was then poured into water and extracted three times with ethyl acetate. The organic layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 0.93 g of 4-chloro-6-(2,3-difluorobenzyl)pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291730B2
Source datasetuspto-grants-2007_11
ORD IDord-95b6c9d84c6c4b7a947685dc16ad683e
Source noteuspto-grants-2007_11