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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912602Generated: November 4, 2026

2,6-Dichlorobenzyl chloride → HCID 22398446, compound

https://huagongshe.com/reaction/912602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichlorobenzyl chlorideHCID 74832—
Reactant2,4,6-TrichloropyrimidineHCID 77378—
ReactantMagnesiumHCID 5462224—
Catalyst1,2-DibromoethaneHCID 7839—
ProductHCID 22398446HCID 2239844621%

Reaction Steps

A solution of 2,6-dichlorobenzylchloride (0.102 mol) in 1,1-diethylether (10 ml) was added dropwise to magnesium (0.102 mol) in 1,1-diethylether (60 ml). The reaction was initiated by adding 2 drops of 1,2-dibromoethane. After most of magnesium disappeared, 2,4,6-trichloropyrimidine (0.051 mol) in 1,1-diethylether (30 ml) was added. The mixture was stirred overnight at room temperature. The solvent was evaporated and the residue was purified by flash column chromatography over silica gel (eluent: CH2Cl2/hexane 1/2). The desired fractions were collected and the solvent was evaporated, yielding 3.3 g of (21%) 2,4-dichloro-6-[(2,6-dichloro-phenyl)methyl]pyrimidine (interm. 1; m.p.: 106-107° C.). b) Intermediate (1) (0.0081 mol) in 2-propanol (100 ml) was heated until complete dissolution. The solution was then transferred into a pressure tube and NH3 gas was bubbled into it for 20 minutes. Then the mixture was heated to 80° C. for 16 hours. The solvent was evaporated, yielding a residue of two compounds: 2-chloro-6-[(2,6-di-chloro-phenyl)methyl]-4-pyrimidinamine (interm. 2) and 4-chloro-6-[(2,6-dichloro-phenyl)methyl]-2-pyrimidinamine (interm. 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026248B2
Source datasetuspto-grants-2011_09
ORD IDord-f854d7387ab74629ac0e06a4bb4a8723
Source noteuspto-grants-2011_09