HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 4-cyano-4-(2,4-difluorophenyl)piperidine-1-carboxylate → 4-(2,4-Difluorophenyl)-piperidine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 4-cyano-4-(2,4-difluorophenyl)piperidine-1-carboxylate | HCID 18353388 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-(2,4-Difluorophenyl)-piperidine-4-carbonitrile | HCID 10513208 | 90% |
Reaction Steps
To 4-Cyano-4-(2,4-difluorophenyl)-piperidine-1-carboxylic acid tert-butyl ester (0.720 g, 2.42 mmol) in 5 ml of dichloromethane, 2 ml of trifluoroacetic acid was added and the solution stirred at room temperature for 1 hour. The solution was concentrated, neutralized with 10% KOH solution and extracted into 25 ml of dichloromethane. The organic layer was dried over sodium sulfate, filtered and concentrated to give 0.484 g (90%) of 4-(2,4-difluorophenyl)-piperidine-4-carbonitrile which was used as such for the subsequent step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06245773B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-9556294d98604d2dbe3c922a4a0f0935 |
| Source note | uspto-grants-2001_06 |