HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 4-[4-(2-Oxazolin-2-yl)benzyl]-1-(4-trifluoromethylbenzoyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-[4-(2-Oxazolin-2-yl)benzylidene]-1-(4-trifluoromethylbenzoyl)piperidine | HCID 15231386 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[4-(2-Oxazolin-2-yl)benzyl]-1-(4-trifluoromethylbenzoyl)piperidine | HCID 15231394 | — |
Reaction Steps
441 mg (1 mmol) of 4-[4-(2-oxazolin-2-yl)benzylidene]-1-(4-trifluoromethylbenzoyl)piperidine are hydrogenated (ambient temperature, 30 minutes, hydrogen pressure 50 psi) in 10 ml of anhydrous ethanol and 2.5 ml of ethyl acetate in the presence of 0.5 g of palladium-carbon (10%). The catalyst is then suction-filtered, the filtrate is evaporated under reduced pressure at a bath temperature of 50° C. and the residue is purified by column chromatography (Silica gel; ethyl acetate). 200 mg (48% of theory) of the title compound of melting point 115° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05466687 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-86e54884df594b6f9f2f01f4ed97cdcc |
| Source note | uspto-grants-1995_11 |