HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902860Generated: October 29, 2026
Ethyl Acetate → 4-(Pyridin-4-yl)benzoic acid hydrochloride
https://huagongshe.com/reaction/902860
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Bromopyridinium chloride | HCID 88100 | — |
| Reactant | 4-Carboxyphenylboric acid | HCID 22709991 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(Pyridin-4-yl)benzoic acid hydrochloride | HCID 57432607 | 64.6% |
Reaction Steps
4-Bromopyridine hydrochloride (11.7 g) and 4-carboxyphenylboric acid (10.0 g) were dissolved in a mixed solvent of toluene (250 ml) and water (250 ml), tetrakis(triphenylphosphine)palladium(0) (5.0 g) and anhydrous sodium carbonate (25.4 g) were successively added, and the mixture was heated under reflux at 120° C. for 19 hours. After the reaction mixture was cooled to room temperature, ethyl acetate was added to the reaction mixture to extract it with water. Concentrated hydrochloric acid was added to the water layer to acidify it. The water layer was washed with ethyl acetate and then concentrated, and solids deposited were collected to obtain the title compound (8.37 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365205B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-bcb80fad52614277a4031695834abf5e |
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| Source note | uspto-grants-2008_04 |
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