HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263957Generated: October 31, 2026
Ethanol → 4-Bromo-2-ethoxy-benzoic acid ethyl ester
https://huagongshe.com/reaction/2263957
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 4-bromo-2-fluorobenzoate | HCID 22031817 | — |
| Product | 4-Bromo-2-ethoxy-benzoic acid ethyl ester | HCID 58894221 | 77% |
Reaction Steps
Sodium (1.815 g, 78.9 mmol, Aldrich) was cut into small pieces and added to ethanol (100 mL). After all the pieces were dissolved, the clear solution was added to a solution of ethyl 4-bromo-2-fluoro-benzoate (13 g, 52.6 mmol) in ethanol (20 mL) cooled to 0° C. The ice bath was then removed and the mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated in vacuo, and the residue was taken in water and 20% ethyl acetate-hexane. The organic layer was washed with saturated solution of sodium bicarbonate, brine, and dried over anhydrous sodium sulfate. The solids were filtered off, and the filtrate was concentrated in vacuo. Purification of the crude residue by flash chromatography (120 g of silica gel, eluting with 10-15% ethyl acetate in hexane) gave 4-bromo-2-ethoxy-benzoic acid ethyl ester as white solids (11.020 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851626B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-9e17f62b135d4aabaa0fe493f69ad151 |
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| Source note | uspto-grants-2010_12 |
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