HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-benzyl-1-phenylethanimine → N-benzyl-1-phenylethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-benzyl-1-phenylethanimine | HCID 297338 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Triethylammonium formate | HCID 11084032 | — |
| Product | N-benzyl-1-phenylethylamine | HCID 519427 | 23% |
Reaction Steps
The catalyst of formula 1.3 (10 μmol) was added to N-benzyl acetophenone imine (1 mmol) and tBuOK (5.6 mg, 50 μmol) was added too. Now 0.5 ml of a HCO2H/Et3N (3:2) mixture was added and the solution was stirred under nitrogen at 400 C for 24 h. After 36 h at ambient temperature 23% N-benzyl-1-phenylethylamine had formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07884223B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-f7e11aea9203461594b2955906c84485 |
| Source note | uspto-grants-2011_02 |