HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Furan-3-yl-5-hydroxy-benzonitrile → 3-Aminomethyl-4-furan-3-yl-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Furan-3-yl-5-hydroxy-benzonitrile | HCID 59300111 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Aminomethyl-4-furan-3-yl-phenol | HCID 59300237 | 72% |
Reaction Steps
The 2-Furan-3-yl-5-hydroxy-benzonitrile obtained above is dissolved in EtOH and to which Raney Ni (1 g of suspension in water) is added. The mixture is then subjected to hydrogenation under H2 (50 psi) for 24 hours. After which Raney Ni is filtered off from celite and EtOH is removed to provide the title compound (40 mg, 72% for two steps). MS (ESI): 190 (M+1)+1, 173 (M+1-NH3)+1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-5d8dbbbb82024049b6a36d5dd8dfd73f |
| Source note | uspto-grants-2010_05 |