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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590376Generated: November 4, 2026

Acetic Acid → 5-Bromonaphthalene-2-carboxylic acid

https://huagongshe.com/reaction/1590376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantIodineHCID 807—
Reactant1-Naphthoic acidHCID 6847—
ReactantBromineHCID 24408—
CatalystBromineHCID 24408—
Product5-Bromonaphthalene-2-carboxylic acidHCID 14960646—

Reaction Steps

To naphthoic acid (50 g) (ex Aldrich) in glacial acetic acid at reflux was added a few drops of bromine (ex BDH) followed by iodine (0.5 g) (ex (BDH). Bromine (15 ml) was added dropwise over one hour. The mixture was cooled to 25° and stirred there for 18 hours. The resulting white precipitate was filtered, dissolved in hot water and treated with concentrated hydrochloric acid. The precipitate was filtered and dried (over phosphorus pentoxide (ex BDH) to give 5-bromo-2-napthoic acid (recrystallised from ethanol) (28 g). Melting point 261°-2°. NMR 1H:(DMSO,CDCl3), 8.60(1H,s), 8.00(5H,m), 7.40(1H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05202356
Source datasetuspto-grants-1993_04
ORD IDord-349a6dae78c1414ca5a23eea3348f7bb
Source noteuspto-grants-1993_04