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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158469Generated: November 3, 2026

Sodium Hydroxide → 4-Methoxy-3-(2-methoxy-ethoxymethyl)-benzoic acid

https://huagongshe.com/reaction/1158469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Methoxy-3-(2-methoxy-ethoxymethyl)-benzoic acid ethyl esterHCID 68616710—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-3-(2-methoxy-ethoxymethyl)-benzoic acidHCID 59512262—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 4-methoxy-3-(2-methoxy-ethoxymethyl)-benzoic acid ethyl ester (0.87 g, 3.24 mmol) in a 1:1 mixture of THF and 4N NaOH (10 mL) is stirred at 50° C. overnight. After cooling, the volatiles are removed at reduced pressure, the remaining aqueous phase is acidified to pH 1 by dropwise addition of HCl 37%, and the resulting suspension is filtered off. The precipitate is washed with water, dried overnight in vacuo to give the title compound. TLC, Rf (hexane/AcOEt 1:1)=0.07. MS: 239.0 [M−H]+. tR (HPLC, Nucleosil C18HD column, 20-100% CH3CN/H2O/6 min, 100% CH3CN/2 min, CH3CN and H2O containing 0.1% TFA, flow: 1 mL/min): 2.71 min. 1H-NMR (DMSO-d6): δ 3.29 (s, 3H), 3.52 (m, 2H), 3.64 (m, 2H), 3.88 (s, 3H), 4.51 (s, 2H), 7.10 (m, 1H), 7.90 (m, 1H), 7.94 (m, 1H), 12.6 (s, br, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807709B2
Source datasetuspto-grants-2010_10
ORD IDord-94f6d7d78532498bb81013bd7e54186d
Source noteuspto-grants-2010_10