HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295921Generated: October 29, 2026
Dimethylformamide → Ethyl 5-bromo-2-ethoxy-4-methylbenzoate
https://huagongshe.com/reaction/1295921
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-bromo-2-hydroxy-4-methylbenzoic acid | HCID 243934 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 5-bromo-2-ethoxy-4-methylbenzoate | HCID 22929763 | — |
Reaction Steps
After dissolving 5-bromo-2-hydroxy-4-methylbenzoic acid (9.35 g) in dimethylformamide, potassium carbonate (14 g) and ethyl iodide (8 ml) were added in that order and the mixture was stirred at 50° C. for 3 hours. It was then diluted with ethyl acetate, washed with water and brine, dried over anhydrous magnesium sulfate, filtered and concentrated to yield ethyl 5-bromo-2-ethoxy-4-methylbenzoate. The product was dissolved in ethanol (100 ml), 5 N sodium hydroxide (20 ml) was added and the mixture was heated to reflux for 30 minutes. After adding 5 N hydrochloric acid (25 ml) for neutralization, extraction was performed with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, filtered and concentrated to yield the title compound (10.4 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244730B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-a77b0601025942b6bf398b731656b7d4 |
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| Source note | uspto-grants-2007_07 |
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