HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1-(4-Amino-3-bromo-phenyl)-cyclopropanecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-(4-Aminophenyl)cyclopropanecarbonitrile | HCID 13826936 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4-Amino-3-bromo-phenyl)-cyclopropanecarbonitrile | HCID 68838261 | 80.1% |
Reaction Steps
To a solution of 1-(4-amino-phenyl)-cyclopropanecarbonitrile (96 mg, 0.60 mmol) in MeCN (3 mL) at 0° C. was added NBS (108 mg, 0.60 mmol) and the reaction was allowed to stir overnight. The reaction was diluted with EtOAc (25 mL) and was then washed with saturated aqueous NaHCO3 (1×25 mL). The organic layer was dried (Na2SO4) and concentrated in vacuo to give 114 mg (80%) of 1-(4-amino-3-bromo-phenyl)-cyclopropanecarbonitrile. The crude product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403804B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-55e16492505e4c3c98431b9fc0e297aa |
| Source note | uspto-grants-2016_08 |