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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097672Generated: October 30, 2026

Hydrochloric Acid → Benzyl 3-iodobenzoate

https://huagongshe.com/reaction/2097672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Iodobenzoic acidHCID 12060—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductBenzyl 3-iodobenzoateHCID 22254461—

Reaction Steps

To a solution of 3-iodobenzoic acid (1.0 equiv) in dry DMF (0.5 M) under argon was added solid potassium carbonate (1.5 equiv) followed by benzyl bromide (1.1 equiv). The resulting mixture was stirred at rt for 4 h, acidified with 10% HCl, diluted with brine and ethyl acetate, and the layers were separated. The organic layer was washed with brine (5×), dried (MgSO4), filtered and concentrated in vacuo to afford a solid, benzyl 3-iodobenzoate (4), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450350B2
Source datasetuspto-grants-2013_05
ORD IDord-e8645a71551c440592818f193c29261a
Source noteuspto-grants-2013_05