HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579779Generated: October 26, 2026
Nitromethane → Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate
https://huagongshe.com/reaction/579779
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Ethyl 4-oxo-1-piperidinecarboxylate | HCID 34767 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate | HCID 22708806 | — |
Reaction Steps
To a stirred and cooled mixture of 85.5 parts of ethyl 4-oxo-1-piperidinecarboxylate, 33.6 parts of nitromethane and 240 parts of methanol were added dropwise 10 parts of a sodium methoxide solution 30% at 10°~15° C. Upon completion, stirring was continued first for 2 hours at about 10° C. and further overnight at room temperature. The reaction mixture was evaporated at room temperature, crushed ice was added to the oily residue and the whole was acidified with acetic acid. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The oily residue was solidified on triturating in petroleum ether. The product was filtered off and dried, yielding 73 parts of ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate (intermediate 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04749702 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-40216e3ef4e545b49a2565aab147c64e |
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| Source note | uspto-grants-1988_06 |
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