HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-benzyl-1-phenylethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-benzyl-1-phenylethanimine | HCID 297338 | — |
| Reactant | HCID 57230745 | HCID 57230745 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-benzyl-1-phenylethylamine | HCID 519427 | — |
Reaction Steps
The process is carried out as in Example 6, but the reaction conditions are modified as follows: 0.636 g (3 mmol) of N-benzyl-N-(1-phenylethylidene)amine, 10.2 mg (0.0152 mmol) of [Ir(1,5-cyclooctadiene)Cl]2, 21.4 mg (0.0333 mmol) of {(R)-1-[(S)-2-diphenylphosphino)ferrocenyl]}ethyl-di(3,5-dimethylphenyl)phosphine (ligand) and 15 mg (0.04 mmol) of tetrabutylammonium iodide, 2 ml of acetic acid, 15 ml of toluene, 30 bar of hydrogen, reaction temperature: 25° C. The reaction time is 20 minutes. The conversion is complete, the ee 31%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06822118B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-2ca8f37cc2294b07b0de46e71d579a36 |
| Source note | uspto-grants-2004_11 |