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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423027Generated: October 26, 2026

Ethyl chloroformate → 1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/423027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantTert-butyl 4-cyanopiperidine-1-carboxylateHCID 1514443—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product1-tert-Butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylateHCID 5775037651.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of LDA (107 ml, 214.01 mmol) was added to a stirred solution of tert-butyl 4-cyanopiperidine-1-carboxylate (30 g, 143 mmol) in THF (250 ml) at −78° C., under nitrogen. The resulting solution was stirred at −78° C. for 30 minutes. Ethyl chloroformate (16.37 ml, 171.2 mmol) was added. The resulting solution was stirred and allowed to warm to room temperature. The reaction mixture was quenched with saturated NaHCO3 (250 ml), extracted with DCM, and the organic layer was washed with saturated brine (100 ml) then dried over MgSO4, filtered and evaporated to afford the crude material as a orange oil. This material was purified by flash silica chromatography, elution gradient 10% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford 1-tert-butyl 4-ethyl 4-cyanopiperidine-1,4-dicarboxylate (20.8 g, 51.6%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101623B2
Source datasetuspto-grants-2012_01
ORD IDord-e521e8be4e0f43de9130e9c71b98b0b5
Source noteuspto-grants-2012_01