HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 87298019, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | N-Ethyl-2,6-dimethylaniline | HCID 12539332 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 87298019 | HCID 87298019 | — |
Reaction Steps
N-ethyl-2,6-dimethylaniline (5.9 g, 39.6 mmol) was added to a stirred solution of cyanogen bromide (2.1 g, 19.8 mmol) in toluene (50 mL). The reaction mixture was allowed to react overnight at room temperature during which a solid formed. A small temperature rise to 30° C. was observed. The suspension was filtered and the residue was washed with toluene (3×25 mL). The combined filtrates were evaporated to dryness by rotatory evaporation and the resulting residue was purified by Kugelrohr distillation (0.2 mbar, 110-125° C.) yielding a brown oil. Yield: 3.09 g (90%). The residue (N-ethyl-2,6-dimethylaniline hydrobromide) of the filtration step was used in the following synthetic step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987393B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-31b0cc3ef0124165a4394cea155ab67f |
| Source note | uspto-grants-2015_03 |