HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → Piperidine, 1-(isocyanoacetyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Methyl isocyanoacetate | HCID 547815 | — |
| Product | Piperidine, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08168631B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-6f75bf929c60479f8b640f1ed717ad4e |
| Source note | uspto-grants-2012_05 |