HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → [(3-Ethylphenyl)amino]carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 3-Ethylaniline | HCID 11475 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | [(3-Ethylphenyl)amino]carbonitrile | HCID 10012043 | 96.5% |
Reaction Steps
A solution of cyanogen bromide (3.31 g, 31.26 mmol) in Et2O (25 ml) was added slowly to a stirred solution of m-ethylaniline (6.06 g, 50 mmol) in Et2O (50 ml) and continued stirring at room temperature for 6 hours. A white precipitate of m-ethylaniline hydrobromide (4.46 g) was filtered off, and the filtrate was washed with H2O (2×20 ml). Evaporation of ether layer afforded the title compound (3.85 g, 96.5%) as a thick liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251948B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-9109bf362e0e4b3fa611fd10a9d0cdfc |
| Source note | uspto-grants-2001_06 |