HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 1-(4-Cyclohexylpiperidin-4-yl)butan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tert-butyl 4-butyryl-4-cyclohexylpiperidine-1-carboxylate | HCID 66987675 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Cyclohexylpiperidin-4-yl)butan-1-one | HCID 66987849 | 119.5% |
Reaction Steps
2.5 g (7.4 mmol) of tert-butyl 4-butyryl-4-cyclohexylpiperidine-1-carboxylate (cf. preparation 17-1-4) are diluted in a mixture comprising 40 mL of dichloromethane and 8 mL of trifluoroacetic acid. The mixture is stirred at room temperature for 2 hours and the reaction is then stopped by adding aqueous 1N NaOH solution and the organic compounds are extracted with dichloromethane. The organic phase is dried and then concentrated. 2.1 g of 1-(4-cyclohexylpiperidin-4-yl)butan-1-one in the form of a colourless oil are obtained in a yield of 100%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877968B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-f99ab9da94334c9b82460196afd9b3f5 |
| Source note | uspto-grants-2014_11 |