HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831764Generated: October 31, 2026
Ethyl Bromide → Ethyl 4-ethoxy-3-hydroxybenzoate
https://huagongshe.com/reaction/1831764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3,4-Dihydroxybenzoate | HCID 77547 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-ethoxy-3-hydroxybenzoate | HCID 11106619 | — |
Reaction Steps
5 g (27.2 mmol) of 3,4-Dihydroxy-benzoic acid ethyl ester was dissolved in 100 ml DMF and 3.75 g (27.2 mmol) of potassium carbonate was added. The solution was cooled to 0° C. and a solution of 2.96 g (27.2 mmol) ethyl bromide in 10 ml DMF was added dropwise. The solution was stirred for 16 h at room temperature (RT). The solvent was removed under reduced pressure. The residue was taken-up in ethyl acetate and the solution was washed three times with water and twice with saturated aqueous sodium chloride. The organic phase was dried with magnesium sulphate, filtered and the solvent was removed under reduced pressure. The residue was chromatographed on silica gel eluting with ethyl acetate/n-heptane (1/4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067665B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-ce3c0dac085d448497c5da2aacc7af88 |
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| Source note | uspto-grants-2006_06 |
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