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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768268Generated: November 1, 2026

Water → Methyl 3-Methoxy-2-naphthoate

https://huagongshe.com/reaction/1768268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-hydroxy-2-naphthoateHCID 70163—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-Methoxy-2-naphthoateHCID 29695295.1%

Reaction Steps

A slurry of methyl 3-hydroxy-2-naphthoate (10.1 g, 50.1 mmol) and K2CO3 (7.96 g, 57.6 mmol) in DMF (200 mL) was stirred at room temp. for 15 min., then treated with iodomethane (3.43 mL, 55.1 mmol). The mixture was allowed to stir at room temp. overnight, then was treated with water (200 mL). The resulting mixture was extracted with EtOAc (2×200 mL). The combined organic layers were washed with a saturated NaCl solution (100 mL), dried (MgSO4), concentrated under reduced pressure (approximately 0.4 mmHg overnight) to give methyl 3-methoxy-2-naphthoate as an amber oil (10.30 g): 1H-NMR (DMSO-d6) δ2.70 (s, 3H), 2.85 (s, 3H), 7.38 (app t, J=8.09 Hz, 1H), 7.44 (s, 1H), 7.53 (app t, J=8.09 Hz, 1H), 7.84 (d, J=8.09 Hz, 1H), 7.90 (s, 1H), 8.21 (s, 1H). Step 2. 3-Methoxy-2-naphthoic acid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235576B1
Source datasetuspto-grants-2007_06
ORD IDord-1bead707131647c8b54677dc43d05266
Source noteuspto-grants-2007_06