HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(2-Cyano-4-methylphenyl)-4-piperidone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-(2-Cyano-4-methylphenyl)-4-piperidone propylene ketal | HCID 86757963 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(2-Cyano-4-methylphenyl)-4-piperidone | HCID 22615416 | — |
Reaction Steps
A solution of 29 (549 mg, 2.00 mmol) in ether (20 mL) was treated with 3N aqueous HCl (25 mL). The mixture was stirred at room temperature (24 h). The solvent was removed in vacuo and the residue dissolved in 6N HCl (25 mL) and acetic acid (10 mL). The mixture was stirred at room temperature (3 h). The reaction mixture was neutralized with sodium carbonate solution and the aqueous layer was extracted with three portions of ether. The combined organic extracts were washed with brine, dried over Na2SO4, and concentrated under reduced pressure to afford the title compound (30).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376503B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-87f8721a71604261af6e2c1230d3796f |
| Source note | uspto-grants-2002_04 |