HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 2-(4-dimethylamino-4-phenyl-cyclohexyl)-N-phenyl-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (4-Dimethylamino-4-phenyl-cyclohexyl)-acetic acid ethyl ester | HCID 67386781 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-dimethylamino-4-phenyl-cyclohexyl)-N-phenyl-acetamide | HCID 11646444 | — |
Reaction Steps
n-Butyllithium (1.6 M solution in hexane; 7.1 ml; 11.4 mmol) was added dropwise at 0° C. to a solution of aniline (0.53 g; 5.7 mmol) in 10 ml THF. The mixture was allowed to come to RT and was subsequently stirred for 1 h. A solution of (4-dimethylamino-4-phenyl-cyclohexyl)-acetic acid ethyl ester (1.5 g; 5.2 mmol) in 15 ml THF was added dropwise at −78° C. The mixture was subsequently stirred for 1 h and then allowed to come to RT. It was hydrolysed with ammonium chloride solution and extracted with MC. After concentration, the crude product was chromatographed on silica gel (eluent:ether). 308 mg (18%) of the less polar and 620 mg (36%) of the more polar diastereoisomer were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08017630B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-5bc8593a3cb0479aa7dc6291ceb75857 |
| Source note | uspto-grants-2011_09 |