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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470617Generated: October 30, 2026

tert-Butyl 4-(cyanomethylidene)piperidine-1-carboxylate → tert-Butyl 4-(cyanomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/470617

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(cyanomethylidene)piperidine-1-carboxylateHCID 15326949—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 4-(cyanomethyl)piperidine-1-carboxylateHCID 22248390—

Reaction Steps

4-Cyanomethylene-piperidine-1-carboxylic acid tert-butyl ester (compound of Example 14; 6.9 g, 31.0 mmol) and Pd/C (0.7 g) in ethanol (150 mL) was maintained under hydrogen atmosphere for 8 h. The reaction mixture was filtered through Celite and the solvent was evaporated to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629277B2
Source datasetuspto-grants-2014_01
ORD IDord-818dcfa918dd4a16a8512cc81129a5aa
Source noteuspto-grants-2014_01