HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (+/-)-1-(1-Amino-3-butyl)-4-(4-fluorophenyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 3-[4-(4-Fluorophenyl)piperidin-1-yl]butanenitrile | HCID 91182868 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (+/-)-1-(1-Amino-3-butyl)-4-(4-fluorophenyl)piperidine | HCID 91338801 | — |
Reaction Steps
A solution of (+/−)-1-(1-cyano-2-propyl)-4-(4-fluorophenyl)piperidine (457 mg, 1.85 mmol) in tetrahydrofuran (5 mL) was added dropwise to 1 M borane/tetrahydrofuran (5 mL) under an inert argon atmosphere. The reaction mixture was refluxed for two hours and then cooled to ambient temperature. 6 N HCl (4 mL) was added to the reaction, stirred for 0.5 hour and then the tetrahydrofuran boiled off. The resultant aqueous solution was cooled in an ice bath and made basic by addition solid sodium hydroxide pellets. The product was extracted into methylene chloride, the extract dried (anhydrous sodium sulfate), filtered, and the solvent removed to give the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06316437B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-e59753223df547fe98a587abbccc430b |
| Source note | uspto-grants-2001_11 |