Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261098Generated: November 2, 2026

Dimethylformamide → 2,3-Bis-(4-chloro-benzyloxy)-benzaldehyde

https://huagongshe.com/reaction/1261098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
Reactant2,3-DihydroxybenzaldehydeHCID 90579—
SolventTetrahydrofuranHCID 8028—
Product2,3-Bis-(4-chloro-benzyloxy)-benzaldehydeHCID 5808730446%

Reaction Steps

To a solution of 2,3-dihydroxybenzaldehyde (626, 2.0 g, 14.5 mmol) in tetrahydrofuran (100 mL) was added sodium hydride (0.52 g, 13.0 mmol) at 0° C. under an atmosphere of nitrogen. The reaction mixture was allowed to warm to room temperature and was stirred at room temperature for 30 minutes. To the reaction mixture was then added 4-chlorobenzyl bromide (557, 2.7 g, 13.0 mmol). The reaction mixture was stirred at room temperature under an atmosphere of nitrogen overnight. N,N-dimethylformamide (50 mL) was added into the reaction mixture and it was stirred at room temperature for 24 hours. The reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layer was collected, washed with brine, and dried over magnesium sulfate. After removal of solvent, the residue was purified by silica gel column chromatography eluting with ethyl acetate in hexane to provide the compound as an off-white solid (627, 2.3 gm, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470818B2
Source datasetuspto-grants-2013_06
ORD IDord-513db8605d1b45bcbaa3d2736fb339b4
Source noteuspto-grants-2013_06