HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336259Generated: October 29, 2026
2-Methylpiperidine → HCID 16771415, compound
https://huagongshe.com/reaction/336259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylpiperidine | HCID 7974 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Chloro-3-pyridinecarbonitrile | HCID 5152094 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 16771415 | HCID 16771415 | — |
Reaction Steps
A mixture of 6-chloronicotinonitrile (Maybridge SPB04745; 1.5 g; 10.8 mmol; 1 eq.) and 2-methylpiperidine (25.6 ml; 216.5 mmol; 20 eq.) was stirred at 90° C. for 24 hours. The mixture was diluted with ethyl acetate, washed with water and brine, dried over magnesium sulphate and concentrated in vacuo. To the residue (1.5 g; 7.45 mmol; 1 eq.) in water (90 mL) was added potassium hydroxide (2.09 g; 37.3 mmol; 5 eq.) and the reaction mixture was refluxed for 16 hours. After cooling to room temperature, the precipitate was filtered off and the filtrate acidified to pH 6 with HCl 1M. The precipitate was filtered off and dried to afford the title compound as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889668B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-4c4c9859c30c4979a20f8ff588207be4 |
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| Source note | uspto-grants-2014_11 |
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