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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantEthyl 4-oxo-1-piperidinecarboxylateHCID 34767—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductEthyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04749702
Source datasetuspto-grants-1988_06
ORD IDord-40216e3ef4e545b49a2565aab147c64e
Source noteuspto-grants-1988_06