HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 3-Amino-α,α-dimethyl-3-phenyl-1-piperidineacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 1236302-98-9 | HCID 59438506 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Amino-α,α-dimethyl-3-phenyl-1-piperidineacetonitrile | HCID 59438523 | 76.1% |
Reaction Steps
To a solution of 300 mg (1.701 mmol) rac-3-Phenyl-piperidin-3-ylamine in 1.3 ml acetic acid, was added dropwise 188 ul (2.553 mmol) acetone. The mixture was stirred at room temperature for 5 minutes. 320 ul (2.553 mmol) trimethylsilyl cyanide was added dropwise. The temperature rose to 31° C. The mixture was stirred at room temperature for 4 hours. The mixture was diluted with dichloromethane and cooled to 0° C. NaOH 2N was added dropwise to basify the mixture. The organic layer was separated and the aqueous layer was extracted twice with dichloromethane. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to provide 315 mg (76.1%) of the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067911B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-cb1bae700b2a45db91f39a283af33159 |
| Source note | uspto-grants-2015_06 |