HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744507Generated: November 1, 2026
Water → Ethyl 1-(4-amino-2-cyanophenyl)-4-piperidinecarboxylate
https://huagongshe.com/reaction/1744507
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 1-(2-cyano-4-nitrophenyl)piperidine-4-carboxylate | HCID 9280152 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1-(4-amino-2-cyanophenyl)-4-piperidinecarboxylate | HCID 22227900 | 77.9% |
Reaction Steps
Ammonium chloride (2.1 g) and iron powder (11.1 g) were added to a mixed solvent of water (110 ml) and ethanol (30 ml), and the mixture was heated to 65° C. Then, ethyl 1-(4-nitro-2-cyanophenyl)piperidin-4-ylcarboxylate (17.1 g) was added in parts over 20 min and the mixture was stirred at a refluxing temperature for 30 min. The reaction mixture was ice-cooled and filtrated. The solvent was evaporated under reduced pressure. To the residue was added aqueous sodium hydroxide solution, and the mixture was extracted with toluene. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate, after which the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the residue to allow crystallization. The crystals were recrystallized from a mixed solvent of ethyl acetate-n-hexane to give the title compound (12 g), melting point: 98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07015218B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-d341ca4ff14f4215998ab865c22c16c5 |
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| Source note | uspto-grants-2006_03 |
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