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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 2-[4-(acetyloxy)-2-methylphenoxy]-2-methylpropanoate | HCID 21986549 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-(4-hydroxy-2-methylphenoxy)-2-methylpropanoate | HCID 16756990 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091237B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-cde935c22f454ba4aabd0f9182db7aa1 |
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| Source note | uspto-grants-2006_08 |
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