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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623649Generated: November 1, 2026

5-Bromosalicylic acid → HCID 67107679, compound

https://huagongshe.com/reaction/1623649

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromosalicylic acidHCID 6972—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Methoxybenzyl bromideHCID 4067207—
SolventAcetoneHCID 180—
ProductHCID 67107679HCID 67107679—

Reaction Conditions

Temperature55 °C

Reaction Steps

Neat 1-(bromomethyl)-3-methoxybenzene (510 mg, 2.53 mmol) was added in one charge to a stirred suspension of 5-bromo-2-hydroxybenzoic acid (250 mg, 1.15 mmol) and potassium carbonate (318 mg, 2.304 mmol) in acetone (40 ml) under nitrogen at 20° C. The reaction mixture was stirred at 55° C. for 16 h. The organic phase was evaporated and the residue was washed with water (25 ml), extracted by ethyl acetate (3×30 ml) and evaporated in vacuo to yield the title compound as an off-white solid. 430 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-34b0e1e372d74ca9bb5d456e5715a221
Source noteuspto-grants-2014_07