HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532479Generated: October 25, 2026
Cyanogen Bromide → 4-Hydroxypiperidine-1-carbonitrile
https://huagongshe.com/reaction/532479
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Hydroxypiperidine-1-carbonitrile | HCID 21897825 | — |
Reaction Steps
Sodium bicarbonate was dissolved in water, and a solution of 4-hydroxypiperidine in dichloromethane and BrCN were added thereto at 0° C. The reaction mixture was stirred at 0° C. for 30 min and further stirred at room temperature for 2 hours. After completion of the reaction, the reaction mixture was extracted twice with dichloromethane. The organic layer thus obtained was dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853213B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-e3fcc2a87400417280fa42596d3f0cbf |
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| Source note | uspto-grants-2014_10 |
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