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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879840Generated: November 1, 2026

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

https://huagongshe.com/reaction/1879840

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 numberUS08318742B2
Source datasetuspto-grants-2012_11
ORD IDord-e0d5f3f34b76432ca5c44b6036f2a842
Source noteuspto-grants-2012_11