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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454457Generated: October 27, 2026

Hydrochloric Acid → Methyl 2-(benzyloxy)-4-iodobenzoate

https://huagongshe.com/reaction/454457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-iodosalicylateHCID 11380407—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductMethyl 2-(benzyloxy)-4-iodobenzoateHCID 66990993—

Reaction Conditions

Temperature80 °C

Reaction Steps

Potassium carbonate (1.9 g) and benzyl bromide (1.2 mL) were sequentially added to an N,N-dimethylacetamide (20 mL) solution of methyl 2-hydroxy-4-iodobenzoate (2.5 g), followed by stirring at 80° C. for 1 hour. The reaction mixture was cooled to room temperature, and then 1 mol/L hydrochloric acid and ethyl acetate were added thereto. The organic layer was separated, washed with 1 mol/L hydrochloric acid and a saturated aqueous solution of sodium chloride sequentially, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [Fuji Silysia Chemical Ltd., PSQ100B (spherical), eluent: 90-80% hexane/ethyl acetate] to obtain 3.3 g of methyl 2-(benzyloxy)-4-iodobenzoate as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-eaf519960013447b88048e93c9cd3ecc
Source noteuspto-grants-2013_07