HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → (4-Amino-3-bromophenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Aminophenylacetonitrile | HCID 77000 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (4-Amino-3-bromophenyl)acetonitrile | HCID 45037053 | 92.2% |
Reaction Steps
A solution of 4-aminophenylacetonitrile (1.45 g, 10.9 mmol) in acetonitrile (10 mL) at 0° C. was treated with NBS (1.95 g, 10.9 mmol) in acetonitrile (10 mL) dropwise via an addition funnel. The reaction was allowed to warm to room temperature and then concentrated in vacuo. The crude product was dissolved in EtOAc (50 mL), washed with saturated aqueous NaHCO3 (2×50 mL) and dried (Na2SO4). Removal of the solvent in vacuo afforded the title compound (2.12 g, 92%) as a reddish solid. Mass spectrum (ESI, m/z): Calcd. for C8H7BrN2, 210.9 (M+H), found 211.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790724B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-1a9296351bdb408a8b5e398ccc402edd |
| Source note | uspto-grants-2010_09 |