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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9628Generated: October 27, 2026

Hydrochloric Acid → Ethyl 2-(4-hydroxy-2-methylphenoxy)-2-methylpropanoate

https://huagongshe.com/reaction/9628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 2-[4-(acetyloxy)-2-methylphenoxy]-2-methylpropanoateHCID 21986549—
SolventEthanolHCID 702—
ProductEthyl 2-(4-hydroxy-2-methylphenoxy)-2-methylpropanoateHCID 16756990—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of ethyl 2-[4-(acetyloxy)-2-methylphenoxy]-2-methylpropanoate (intermediate 9, 40.8 g) in ethanol (280 ml) was treated with sodium ethoxide (12.9 g) at room temperature under nitrogen. The resulting solution was heated to 50° C. for 1 hour. 2M hydrochloric acid (95 ml) was added to the cooled reaction and the solution concentrated. The residue was dissolved in t-butylmethyl ether and the resulting solution washed with water followed by brine and then dried over sodium sulfate, filtered and the filtrate concentrated to give a brown oil. Further purification by Biotage® chromatography eluting initially with cyclohexane and then cyclohexane:ethyl acetate (5:1) gave the title compound as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091237B2
Source datasetuspto-grants-2006_08
ORD IDord-cde935c22f454ba4aabd0f9182db7aa1
Source noteuspto-grants-2006_08