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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623635Generated: October 31, 2026

5-Bromosalicylic acid → HCID 67106908, compound

https://huagongshe.com/reaction/1623635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromosalicylic acidHCID 6972—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
SolventAcetoneHCID 180—
ProductHCID 67106908HCID 67106908—

Reaction Conditions

Temperature55 °C

Reaction Steps

1-(Bromomethyl)-4-chlorobenzene (592 mg, 2.88 mmol) was added in a single charge to a stirred suspension of 5-bromo-2-hydroxybenzoic acid (250 mg, 1.15 mmol) and potassium carbonate (478 mg, 3.46 mmol) in acetone (40 ml) under nitrogen at 20° C. The reaction mixture was stirred at 55° C. for 18 h. The organic phase was evaporated and the residue was washed with water (25 ml), extracted with ethyl acetate (30×3 ml) and evaporated in vacuo to yield the title compound as an off-white solid. 320 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-e1600262c5264bc9a32edb78a2f31b74
Source noteuspto-grants-2014_07