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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623637Generated: October 30, 2026

5-Bromosalicylic acid → HCID 67107142, compound

https://huagongshe.com/reaction/1623637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromosalicylic acidHCID 6972—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methoxybenzyl bromideHCID 165021—
SolventAcetoneHCID 180—
ProductHCID 67107142HCID 67107142—

Reaction Conditions

Temperature55 °C

Reaction Steps

1-(Bromomethyl)-4-methoxybenzene (510 mg, 2.53 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 (318 mg, 2.30 mmol) in acetone (40 ml) over 1 min under nitrogen. 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 with ethyl acetate (3×30 ml) and evaporated in vacuo to yield the title compound as a light yellow solid. 400 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-d96f3ed5948a45db86e7db2ece442129
Source noteuspto-grants-2014_07