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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185885Generated: October 26, 2026

Oxalyl chloride → Methyl 3-hydroxynaphthalene-1-carboxylate

https://huagongshe.com/reaction/2185885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-Hydroxy-1-naphthoic acidHCID 190232—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-hydroxynaphthalene-1-carboxylateHCID 2342309035%

Reaction Steps

To a stirred solution of 3-hydroxy-1-naphthalenecarboxylic acid (6.67 g, 35.4 mmol) and oxalyl chloride (3.86 mL, 44.2 mmol) in DCM (150 mL) was added 3 drops of DMF. The mixture was stirred at room temperature for 3 h., the solvent was removed under reduced pressure and methanol (150 mL) was added. After stirring at reflux for 15 min the solvent was removed under reduced pressure, the residue was purified by column chromatography (10%, 20% and 30% EtOAc/hexane) to give the title compound as a yellow solid (2.5 g, 35%). 1H NMR (DMSO-d6) δ 10.10 (s, 1H), 8.61 (d, 1H), 7.77 (d, 1H), 7.72 (d, 1H), 7.47 (m, 2H), 7.38 (d, 1H), 3.93 (s, 3H); MS m/z 201.1 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403601B1
Source datasetuspto-grants-2002_06
ORD IDord-6f31a575f07b468da6155b9f28e6b5a0
Source noteuspto-grants-2002_06