HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049415Generated: October 30, 2026
Hydrochloric Acid → 3-[(1E)-3-ethoxy-3-oxoprop-1-en-1-yl]benzoic acid
https://huagongshe.com/reaction/1049415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | 3-Iodobenzoic acid | HCID 12060 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[(1E)-3-ethoxy-3-oxoprop-1-en-1-yl]benzoic acid | HCID 10489084 | 104.3% |
Reaction Steps
Under an argon atmosphere, to a solution of 3-iodobenzoic acid (20.2 g) in DMF (130 mL) were added ethyl acrylate (9.00 g), triethylamine (24 mL) and palladium (II) acetate (92 mg), and the mixture was stirred at 140° C. for 3 hr. The reaction mixture was cooled to room temperature, and 1N hydrochloric acid was added. The reaction mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (18.7 g) as an orange amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382188B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-65885fc2b90f40a78bc3f45896a258d5 |
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| Source note | uspto-grants-2016_07 |
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