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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166791Generated: October 26, 2026

Methanol → Methyl 5-bromo-1-naphthoate

https://huagongshe.com/reaction/1166791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant5-Bromonaphthalene-1-carboxylic acidHCID 697605—
ProductMethyl 5-bromo-1-naphthoateHCID 455767392%

Reaction Steps

To a suspension of 5-bromo-1-naphthylcarboxylic acid (5 g, 20 mmol) in 200 mL anhydrous MeOH was added 5 mL concentrated H2SO4 and refluxed overnight. The reaction was cooled to room temperature and concentrated to one-third the volume. The residue was diluted with water and extracted with diethyl ether. The organic layer was separated and washed with water (2×), dried over MgSO4, and concentrated. Silica gel column chromatography using hexane/ethyl acetate (2/11) gave 4.91 g (92%) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613942B1
Source datasetuspto-grants-2003_09
ORD IDord-aba7faf794b04d7faf03e077913ee7f3
Source noteuspto-grants-2003_09