HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(Bromomethyl)-2-fluorobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Fluoro-3-methylbenzonitrile | HCID 23160359 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(Bromomethyl)-2-fluorobenzonitrile | HCID 66678465 | 70.2% |
Reaction Steps
NBS (1.729 g, 9.71 mmol) was added to a solution of 2-fluoro-3-methylbenzonitrile (1.25 g, 9.25 mmol) in acetonitrile (25 mL). The obtained mixture was refluxed, and then benzoic peroxyanhydride (0.045 g, 0.18 mmol) was added. The reaction mixture was refluxed overnight, then cooled to r.t. and water was added. The aqueous phase was discarded and the organic phase was dried over MgSO4 and concentrated. The crude product was purified by flash chromatography using a gradient of EtOAc in heptane as eluent to give the title compound (1.39 g, 70% yield): 1H NMR (500 MHz, DMSO-d6) δ ppm 4.75 (s, 2H) 7.43 (t, 1H) 7.93 (t, 2H); MS (EI) m/z 213 M+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09248129B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-91876803bc8b42a2b000d75e113a2814 |
| Source note | uspto-grants-2016_02 |