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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592263Generated: October 30, 2026

Water → HCID 22599726, compound

https://huagongshe.com/reaction/1592263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4,6-DichloropyrimidineHCID 70943—
Reactant2-Bromobenzyl bromideHCID 76965—
ReactantTmsciHCID 131723440—
Catalyst1,1-DibromoethaneHCID 11201—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22599726HCID 2259972630.4%

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 2.0 g of 2-bromobenzyl 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 L). 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 L 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 0.69 g of 4-chloro-6-(2-bromobenzyl)pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291730B2
Source datasetuspto-grants-2007_11
ORD IDord-1fee00a8dbd4418f8a8d3316769d9a13
Source noteuspto-grants-2007_11