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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289551Generated: November 1, 2026

Lithium diisopropylamide → Ethyl 4-methylpiperidine-4-carboxylate

https://huagongshe.com/reaction/2289551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-Benzyl 4-ethyl piperidine-1,4-dicarboxylateHCID 15289672—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 4-methylpiperidine-4-carboxylateHCID 19361805—

Reaction Steps

4-Methyl-4-ethoxycarbonyl-piperidine was prepared by alkylation of 1-(benzyloxycarbonyl)-4-ethoxycarbonyl-piperidine (J.Med.Chem 1994, 37, p 368)-2.6 g (10 mmol) 1. in 25 ml dry THF at -70° C., under argon, treated with 7 ml lithium di-isopropylamide solution (2M). Stirred 1.5 hours then a solution of 1.5 equivalents of alkyl halide in 5 ml of THF added dropwise. Reaction allowed to warm to ambient temperature over several hours, diluted with ethyl acetate and water. Aqueous layer extracted twice with ethyl acetate, organic solution washed with brine and dried. Evaporated to give the liquid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093718
Source datasetuspto-grants-2000_07
ORD IDord-ebee02998eeb43ceb7df329971dd7d51
Source noteuspto-grants-2000_07