HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → Phenylcyanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Phenylcyanamide | HCID 69318 | — |
Reaction Steps
To a solution of BrCN (0.11 g, 1.1 mmol) in MeOH (10 mL) at 0° C. was added solid KOAc (0.32 g, 3.3 mmol) and a solution of aniline (0.1 mL, 1.1 mmol) in MeOH (1 mL). The reaction was stirred for 3 hours then partitioned with water (15 mL) and dichloromethane (25 mL). The organic layer was separated, washed with brine, dried over magnesium sulfate, filtered and reduced to dryness to afford N-phenylcyanamide, which was immediately used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754071B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-63a6eeebb60242dc81153c9afdc9727c |
| Source note | uspto-grants-2014_06 |