HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876413Generated: October 29, 2026
Methylhydroquinone → Ethyl (4-hydroxy-3-methylphenoxy)acetate
https://huagongshe.com/reaction/1876413
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylhydroquinone | HCID 7253 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl (4-hydroxy-3-methylphenoxy)acetate | HCID 59419846 | — |
Reaction Steps
A mixture of 2-methylbenzene-1,4-diol (5 g, 40.2 mmol), ethyl 2-bromoacetate (1.1 eq.), and potassium carbonate (2 eq.) in acetonitrile (50 mL) was heated at 80° C. for 18 hours. The reaction was cooled to room temperature, and the acetonitrile was removed in vacuo. Water was added and the crude residue was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography (0-100% EtOAc in hexanes) to provide ethyl 2-(4-hydroxy-3-methylphenoxy)acetate (682) as a pink solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309600B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-1e0be0eca28e4cb19652333095f06874 |
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| Source note | uspto-grants-2012_11 |
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