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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281102Generated: November 3, 2026

Nitromethane → Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/1281102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitromethaneHCID 6375—
ReactantEthyl 4-oxo-1-piperidinecarboxylateHCID 34767—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductEthyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylateHCID 2270880662.9%

Reaction Steps

To a stirred and cooled mixture of ethyl 4-oxo-1-piperidinecarboxylate (85.5 g), nitromethane (33.6 g) in methanol (240 ml), sodium methoxide (10 g) is added dropwise. Upon completion, stirring is continued for 2 hours at about 10° C. and further overnight at room temperature. The reaction mixture is evaporated at room temperature, crushed ice is added to the oily residue and the whole is acidified with acetic acid. The product is extracted with trichloromethane, the extract is dried, filtered and evaporated. The oily residue solidifies on triturating in petroleumether. The product is filtered off and dried, yielding 73 g of ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate (interm. 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06452013B1
Source datasetuspto-grants-2002_09
ORD IDord-1b42f7338cc749d8b01b8914cc650dc8
Source noteuspto-grants-2002_09