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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199097Generated: October 30, 2026

Methanol → (3,5-Dimethyl-4-hydroxy-phenyl)-acetic acid methyl ester

https://huagongshe.com/reaction/2199097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant(4-Hydroxy-3,5-dimethylphenyl)acetic acidHCID 16767514—
Product(3,5-Dimethyl-4-hydroxy-phenyl)-acetic acid methyl esterHCID 2058279886%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of (3,5-dimethyl-4-hydroxy-phenyl)-acetic acid (5a) (12.4 g, 0.069 mmol) in methanol (300 mL) was treated with concentrated sulfuric acid (6.25 mL). The resulting solution was heated to 70° C. overnight. At this time, the reaction was cooled to room temperature. The reaction was concentrated under vacuum. The residue was diluted with ethyl acetate (700 mL) and was washed with water (2×250 mL). The organics were dried over magnesium sulfate, filtered and concentrated under vacuum to give an orange solid. The solid was slurried in 10% ethyl acetate/petroleum ether and was stirred for 1 h. The solid was collected by filtration, washed with 10% ethyl acetate/petroleum ether, and dried under vacuum overnight. The residue was purified by column chromatography using silica gel eluted with 10-15% ethyl acetate in petroleum ether to afford (3,5-dimethyl-4-hydroxy-phenyl)-acetic acid methyl ester (6a) (1.93 g, 86%) as an off-white solid; EI(+)-HRMS m/z calcd for C11H14O3 (M+) 194.0943, found 191.0942. Molecular Weight=194.2324; Exact Mass=194.0943

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE046024E1
Source datasetuspto-grants-2016_06
ORD IDord-b995ee36594744a5864ab92136b5d12d
Source noteuspto-grants-2016_06