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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459148Generated: October 26, 2026

Lithium Hydroxide → 3-(4-Hydroxy-3-methoxyphenyl)-2-methoxypropanoic acid

https://huagongshe.com/reaction/459148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactant3-(4-Hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid methyl esterHCID 58823008—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Hydroxy-3-methoxyphenyl)-2-methoxypropanoic acidHCID 1844366274%

Reaction Steps

A 1N aqueous lithium hydroxide solution was added to a solution of 3-(4-hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid methyl ester (280 mg, 1.17 mmol) in THF at room temperature, and the reaction mixture stirred overnight. The aqueous phase was extracted with ethyl acetate (20 mL), acidified to pH 2, and extracted with ethyl acetate (3×15 mL). The later organic layers were combined and washed with water (15 mL) and brine (10 mL), dried (MgSO4), filtered, and concentrated under vacuum to produce 3-(4-hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid as an oil (183 mg, 74%). 1H-NMR (250.13 MHz, CDCl3): δ 6.83 (1H, d, J=7.8), 6.74 (1H, s), 6.72 (1H, d, J=7.8), 3.99 (1H dd, J=7.8, 4.0), 3.85 (s, 3H), 3.40 (s, 3H), 3.09 (1H, dd, J=14.2, 4.0), 2.91 (1H dd, J=14.2, 7.8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192982B2
Source datasetuspto-grants-2007_03
ORD IDord-2d4d67a8859f406389ddf0bfde39991c
Source noteuspto-grants-2007_03