HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664794Generated: November 1, 2026
Potassium Cyanide → Benzyl 4-cyano-4-(methylamino)piperidine-1-carboxylate
https://huagongshe.com/reaction/1664794
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | Benzyl 4-cyano-4-(methylamino)piperidine-1-carboxylate | HCID 67440047 | — |
Reaction Steps
A solution of potassium cyanide (2.79 g, 42.9 mmol) in water (5 mL) was added to a solution of benzyl 4-oxopiperidine-1-carboxylate (10.0 g, 42.9 mmol) and methylamine hydrochloride (2.90 g, 42.9 mmol) in water/methanol (1:1; 10 mL) at 0° C. The reaction mixture was allowed to warm to ambient temperature. After 48 h, additional methylamine hydrochloride (1.45 g, 21.4 mmol) was added. After 18 h, the mixture was diluted with ether, and extracted with ethyl acetate (3×). The combined organic extracts were dried over magnesium sulfate and concentrated down to 50 mL volume. HCl gas was bubbled to this solution for 5 min. The solid precipitated out of the solution was filtered and washed with ether (3×), ethyl acetate (3×) and dried under reduced pressure to give the hydrochloride salt of the title compound. MS 274.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039460B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-41754674cd3749fb9cb9f127ffd400a3 |
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| Source note | uspto-grants-2011_10 |
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