HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022369Generated: October 25, 2026
Sodium Cyanide → 4-Amino-1-methoxy-piperidine-4-carbonitrile
https://huagongshe.com/reaction/1022369
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Methoxypiperidin-4-one | HCID 19936653 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | 4-Amino-1-methoxy-piperidine-4-carbonitrile | HCID 59614594 | 68.7% |
Reaction Steps
To 10 g of N-methoxy-4-piperidone (J. Org. Chem. 1961, 26, 1867-74) in 240 ml ammoniumhydroxide 25% in water there are added 6.2 g of ammoniumchloride and 4.6 g of sodium cyanide. After stirring for 18 h at 25° C. the reaction mixture is diluted with 200 ml water and extracted with ethyl acetate. The organic phase is separated, dried over sodium sulphate, filtered and evaporated. 8.25 g of 4-amino-1-methoxy-piperidine-4-carbonitrile is obtained as light brow oil, which is used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722578B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-f4e338df5ee04a02bd6e4dab3868329c |
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| Source note | uspto-grants-2014_05 |
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