HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459459Generated: November 1, 2026
Ethanol → Ethyl 4-[amino(hydroxyimino)methyl]-1-piperidinecarboxylate
https://huagongshe.com/reaction/1459459
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Ethyl 4-cyanopiperidine-1-carboxylate | HCID 4060541 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-[amino(hydroxyimino)methyl]-1-piperidinecarboxylate | HCID 54150879 | 47% |
Reaction Steps
Ethanol (150 ml) was added to a solution of hydroxylamine hydrochloride (17.25 g) in water (48 ml). Ethyl 4-cyano-1-piperidinecarboxylate (45 g) was added and the mixture was cooled. Sodium methoxide (44.4 g) was added dropwise at RT and the reaction mixture was stirred for 30 minutes at 60° C. The reaction mixture was cooled, filtered and the filtrate evaporated. The residue was purified by column chromatography on silica gel (eluent: CH2Cl2 /CH3OH 95/5). The pure fractions were collected and the solvent evaporated, yielding 25 g (40%) of ethyl 4-[amino(hydroxyimino)methyl]-1-piperidinecarboxylate. This fraction was redissolved in 2-propanone and converted into the hydrochloric acid salt (1:1) with HCl/2-propanol. The precipitate was filtered off and dried, yielding 22 g (35%) of ethyl 4-[amino(hydroxyimino)methyl]-1-piperidine-carboxylate hydrochloride (intermediate 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05854261 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-09199164904446ca90d349309dcc1eb3 |
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| Source note | uspto-grants-1998_12 |
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