HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129803Generated: October 25, 2026
Hydrochloric Acid → Ethyl 3-(4-aminophenyl)propanoate
https://huagongshe.com/reaction/129803
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 4-nitrocinnamate | HCID 1268038 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-(4-aminophenyl)propanoate | HCID 10442595 | 86.2% |
Reaction Steps
A 500 mL Parr hydrogenation vessel was charged with 12.36 g (55.9 mmol) of (E)-3-(4-nitrophenyl)-2-propenoic acid, ethyl ester, 100 mL of absolute ethanol, 15 mL of concentrated hydrochloric acid and 0.75 g of 10% palladium-on-activated charcoal. The slurry was purged with nitrogen and then agitated under an initial pressure of 44.5 psi of hydrogen gas. After 16 h, 18.5 psi had been consumed. The flask was evacuated, purged again with nitrogen and the contents filtered through Celite and evaporated. The residue was dissolved in water and adjusted to pH 9 with solid sodium carbonate. The resulting mixture was extracted thrice with dichloromethane and the combined organic extracts dried over Na2SO4, filtered and evaporated to provide 9.31 g, 86% of title compound as a yellow oil, sufficiently pure for use in subsequent reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05470845 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-c3aa5048b97b44faa1a154a016bbab21 |
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| Source note | uspto-grants-1995_11 |
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