HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-(3-Nitrophenyl)ethan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Nitrophenethyl azide | HCID 22457534 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3-Nitrophenyl)ethan-1-amine | HCID 12950066 | 80.8% |
Reaction Steps
A mixture of 3-nitrophenethyl azide (0.9 g, 4.69 mmol), triphenyl phosphine (1.22 g, 4.66 mmol) and CH2Cl2 (80 mL) is stirred at room temperature for 3 days. Solvent is removed and the residue is taken up in EtOH (20 mL). The solution is heated to 70° C., added 2M NaOH aqueous solution (10 mL) and stirred at room temperature for 2 hrs. A 10% HCl aqueous solution (20 mL) is then added and refluxed for 2 hrs. After the mixture cool to room temperature, it is washed with benzene, basified with 5N NaOH to pH˜12, extracted with ethyl acetate. The organic layer is dried over Na2SO4 and concentrated to give the product (0.63 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294529B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-ec5f274b9a754f74a9ae132f48149ec3 |
| Source note | uspto-grants-2001_09 |