HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473769Generated: October 30, 2026
Potassium Cyanide → 4-Hydroxyamino-1-methoxy-piperidine-4-carbonitrile
https://huagongshe.com/reaction/1473769
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 1-Methoxy-piperidin-4-one oxime | HCID 58428007 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Hydroxyamino-1-methoxy-piperidine-4-carbonitrile | HCID 86657464 | — |
Reaction Steps
To a suspension of 1-methoxy-piperidin-4-one oxime (240 g, 1.66 mol) and potassium dihydrogen phosphate (792.9 g, 5.83 mol) in water (200 ml) at 0-5° C. was added a solution of potassium cyanide (195.1 g, 3.0 mol) in water (200 ml) dropewise (caution!). The reaction mixture was stirred at room temperature overnight (stoppered flask), treated with another portion of potassium dihydrogen phosphate (79.3 g, 0.58 mol) and further stirred at room temperature over another night. The mixture was flushed with nitrogen, the semi-solid removed by filtration and dissolved in ethyl acetate. The aqueous layer was extracted twice with ethyl acetate, all organic layers combined, washed with water and brine, dried over sodium sulfate and concentrated. The residue was triturated with cold diethyl ether, filtered and dried. Yield: 230.8 g of 4-hydroxyamino-1-methoxy-piperidine-4-carbonitrile as a tan solid, mp 130-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018135B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-a716cde1ffed4402ac84d05757851dba |
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| Source note | uspto-grants-2015_04 |
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