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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070576Generated: October 27, 2026

Methanol → 3-(4-Hydroxyphenyl)-4,4-dimethoxy butyric acid methyl ester

https://huagongshe.com/reaction/2070576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
Reactant4-Oxo-3-[4-(tetrahydropyran-2-yloxy)-phenyl]-butyric acid methyl esterHCID 57771437—
Product3-(4-Hydroxyphenyl)-4,4-dimethoxy butyric acid methyl esterHCID 57771503—

Reaction Steps

To a solution of 4-oxo-3-[4-(tetrahydropyran-2-yloxy)-phenyl]-butyric acid methyl ester (1.29 g) obtained in Step 3 in methanol (13 mL) was added camphorsulfonic acid (98 mg), followed by stirring the reaction mixture at room temperature for 6 hours. Then, after addition of 1N aqueous sodium hydroxide solution (0.42 mL), the reaction mixture was concentrated. To the residue was added water, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, dried and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane (volume ratio)=1:2 to 2:3) to give 3-(4-hydroxyphenyl)-4,4-dimethoxy butyric acid methyl ester (0.99 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299296B2
Source datasetuspto-grants-2012_10
ORD IDord-1a816049059c46fbb238a5ed2dfcd97a
Source noteuspto-grants-2012_10