Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919316Generated: October 25, 2026

Piperidine → Piperidine, 1-(isocyanoacetyl)-

https://huagongshe.com/reaction/1919316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantMethyl isocyanoacetateHCID 547815—
ProductPiperidine, 1-(isocyanoacetyl)-HCID 6455474—

Reaction Steps

To stirred and cooled (0° C.) methyl 2-isocyanoacetate (96% technical grade, 2.46 g, 24.63 mmol) was slowly added piperidine (3.22 mL, 37.85 mmol). The mixture was stirred for 1 h with continuous stirring at room temperature and then concentrated. The residue was dissolved in dichloromethane (50 mL) and the organic layer was washed with 10% aqueous citric acid (2×25 mL), dried over MgSO4, filtered and evaporated. 2-Isocyano-1-(piperidin-1-yl)ethanone, SLA 07116B, was obtained as an orange solid (3.13 g, 83% yield) that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168631B2
Source datasetuspto-grants-2012_05
ORD IDord-6f75bf929c60479f8b640f1ed717ad4e
Source noteuspto-grants-2012_05