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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558166Generated: October 26, 2026

3,4-Dichlorobenzyl chloride → 4-(3,4-Dichlorobenzyloxy)-3-methylbenzaldehyde

https://huagongshe.com/reaction/558166

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxy-3-methylbenzaldehydeHCID 139901—
SolventDimethylformamideHCID 6228—
Product4-(3,4-Dichlorobenzyloxy)-3-methylbenzaldehydeHCID 2307334199.8%

Reaction Steps

0.5M solution of 4-chloromethyl-1,2-dichloro-benzene (1.55 g, 8.0 mmol) in DMF was added dropwise to a suspension of 4-hydroxy-3-methyl-benzaldehyde (990 mg, 7.3 mmol), K2CO3 (1.51 g, 11 mmol) and KI (120 mg, 0.73 mmol) in DMF (100 ml). The reaction mixture was treated as described in Example 6. The residue was purified on silica gel, obtaining 2.15 g of the title compound in a quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063039B2
Source datasetuspto-grants-2011_11
ORD IDord-ceb9bf25bb54464b82e1e54f2003aab6
Source noteuspto-grants-2011_11