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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494644Generated: October 25, 2026

Pyridine → Isopropyl 2-methoxy-1-naphthoate

https://huagongshe.com/reaction/494644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantIsopropanolHCID 3776—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Methoxy-1-naphthoic acidHCID 70356—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductIsopropyl 2-methoxy-1-naphthoateHCID 68874473—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-methoxynaphthoic acid (458 mg, 2.3 mmol) in dry dichloromethane (9 mL) at 0° C. under a N2 atmosphere was added oxalyl chloride (1.4 mL of a 2M solution in dichloromethane, 2.8 mmol) and 4 drops of N,N-dimethyl formamide. The mixture was stirred at 0° C. for 20 minutes then allowed to warm to room temperature and stirred for one hour. The mixture was concentrated in vacuo. To this dry powder was added isopropanol (9 mL) and pyridine (367 μL, 4.5 mmol), with stirring. After stirring for 2 hours at room temperature, the mixture was concentrated and partitioned between H2O (10 mL) and ethyl acetate (3× 10 mL) and the combined organic layers was washed with saturated NaCl (10 mL). The organic layer was dried over Na2SO4, and the crude product was purified by column chromatography on silica gel using 10% ethyl acetate in hexane. The title compound was obtained as a colorless solid (260 mg, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538105B2
Source datasetuspto-grants-2009_05
ORD IDord-3f0a47e72f234e2b844744c7afd38f7e
Source noteuspto-grants-2009_05