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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760614Generated: November 1, 2026

Methanol → Methyl 5-bromonaphthalene-2-carboxylate

https://huagongshe.com/reaction/1760614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Bromonaphthalene-2-carboxylic acidHCID 14960646—
ProductMethyl 5-bromonaphthalene-2-carboxylateHCID 1347702269%

Reaction Steps

5-Bromo-2-naphthoic acid (17.33 g, 69 mmol) and 250 mL of MeOH were combined in a flask under N2 atmosphere. Thionyl chloride (5.84 mL, 80 mmol) was added dropwise over 15 minutes at a temperature of 25-30° C. resulting in a pale yellow mixture. The mixture was heated at reflux for 3¼ hours. The resulting yellow solution was concentrated in vacuo to 137.4 g of solution then placed in the freezer overnight. The resulting thick mixture was filtered and the solid was washed with 100 mL of cold MeOH. The solid was dried in vacuo at 50° C. to give 11.39 g of intermediate title compound as white crystals. A second crop was filtered and washed with 100 mL of cold MeOH. The solid was dried to 1.31 g of white crystals. Yield: 69%, 2 crops.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06844344B2
Source datasetuspto-grants-2005_01
ORD IDord-758b869c041444169d91d29332307d28
Source noteuspto-grants-2005_01