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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355409Generated: October 28, 2026

Benzyl Chloride → 3,5-Difluoro-2,4-dibenzyloxybenzaldehyde

https://huagongshe.com/reaction/355409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Difluoro-2,4-dihydroxybenzaldehydeHCID 18942327—
SolventAcetoneHCID 180—
Product3,5-Difluoro-2,4-dibenzyloxybenzaldehydeHCID 18942322—

Reaction Steps

To a 0.1M solution of Compound 13 (1.0 eq) in acetone is added benzyl chloride (4.0 eq) and anhydrous K2CO3 (7.0 eq). The mixture is heated to reflux for 8 hours and filtered. The filtrate is concentrated in vacuo, and the residue is dissolved in EtOAc. The resulting solution is washed with 3% HCl, washed with brine, dried over anhydrous MgSO4, and concentrated in vacuo. The residue is recrystallized from MeOH to yield Compound 23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05830912
Source datasetuspto-grants-1998_11
ORD IDord-859e2011bfca461496c39b018267b274
Source noteuspto-grants-1998_11