HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-4-ol → 2-(4-Hydroxypiperidin-1-yl)-5-nitrobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | 2-Chloro-5-nitrobenzonitrile | HCID 85504 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Hydroxypiperidin-1-yl)-5-nitrobenzonitrile | HCID 17221373 | 76.7% |
Reaction Steps
2-chloro-5-nitrobenzonitrile (36 g) and 4-hydroxypiperidine (50 g) were added to ethanol (300 ml), and the mixture was stirred at a refluxing temperature for 1 h. The solvent was evaporated under reduced pressure. Diisopropyl ether was added to the residue to allow crystallization. The crystals were recrystallized from hydrous ethanol to give 5-nitro-2-(4-hydroxypiperidin-1-yl)benzonitrile (37.4 g), melting point: 114–115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07015218B1 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-ce0c44999786402aae8feda816941823 |
| Source note | uspto-grants-2006_03 |