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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221289Generated: November 1, 2026

Iodine → 5-Bromonaphthalene-2-carboxylic acid

https://huagongshe.com/reaction/2221289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-Naphthoic acidHCID 7123—
ReactantBromineHCID 24408—
SolventAcetic AcidHCID 176—
Product5-Bromonaphthalene-2-carboxylic acidHCID 1496064653.4%

Reaction Steps

To a boiling solution of 2-naphthoic acid (10.00 g, 58.14 mmol) in acetic acid (50 mL) is added dropwise bromine (3 mL) containing iodine (0.25 g). After the addition is complete, the solution is refluxed for 0.5 hr. A white precipitate forms during cooling and is isolated by filtration, washed with acetic acid and then water. The solid is triturated in methanol (100 mL) and 7.01 g (53.4% yield) of the desired product is obtained as a white solid. m.p. 248-250° C. 1H NMR (300 MHz, CD3OD): δ 8.94 (d, J=1.8 Hz, 1H), 8.52-8.42 (m, 3H), 8.27 (dd, J=1.8, 7.5 Hz, 1H), 7.79 (t, J=8.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368462B1
Source datasetuspto-grants-2008_05
ORD IDord-49889830defc4e909a60fd35f4a4cc42
Source noteuspto-grants-2008_05