HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrophenylacetonitrile → (3-Amino-phenyl)-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrophenylacetonitrile | HCID 12125 | — |
| Catalyst | Iron | HCID 23925 | — |
| Product | (3-Amino-phenyl)-acetonitrile | HCID 4847850 | — |
Reaction Steps
A solution of 3-nitrophenyl acetonitrile (500 mg, 3.1 mmol) in 5% ACOH (10 ml) was heated to 80° C. Iron powder (1.5 g, 27 mmol) was then added and the resulting mixture stirred for 2 h. The reaction mixture was filtered through celite and the filter cake washed with MeCN (4×50 ml). The combined MeCN layers were evaporated in vacuo and the residue was re-dissolved in EtOAc (30 ml) followed by 2M HCl (30 ml). The aqueous layer was separated, basified to pH 10 with 6M NaOH, and extracted with EtOAc (3×80 ml). The combined organic layers were dried (MgSO4), filtered and the solvent removed in vacuo to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662839B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-cd28feba9d29476f811ddb95cd1e1540 |
| Source note | uspto-grants-2010_02 |