HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Amino-5-iodo-2-(trifluoromethyl)benzonitrile → 4-Amino-5-cyano-2-trifluoromethyl-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Amino-5-iodo-2-(trifluoromethyl)benzonitrile | HCID 25067377 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 4-Amino-5-cyano-2-trifluoromethyl-benzonitrile | HCID 16756857 | — |
Reaction Steps
4-Amino-5-iodo-2-trifluoromethyl-benzonitrile (1.5 mmoL), CuCN (1.7 mmoL) in NMP (10 mL) was heated at 150° C. for 4 hrs. The reaction mixture was passed through a pad of Celite. The reaction mixture was then partitioned between ethyl acetate and water. The organic layer was washed with water, then brine, dried over anhydrous Na2SO4, filtered and concentrated to yield the title compound as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088811B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-b56a3338f3874626bcdb1c66268405ee |
| Source note | uspto-grants-2012_01 |