HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 1-{[3-(Bromomethyl)-6-chloro-2-fluorophenyl]oxy}naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-[(6-Chloro-2-fluoro-3-methylphenyl)oxy]naphthalene | HCID 68488277 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-{[3-(Bromomethyl)-6-chloro-2-fluorophenyl]oxy}naphthalene | HCID 68485558 | 45.5% |
Reaction Steps
To a solution of 1-[(6-chloro-2-fluoro-3-methylphenyl)oxy]naphthalene (1.69 g, 5.89 mmol) in carbon tetrachloride (20 mL) was added N-bromosuccinimide (1.154 g, 6.48 mmol) and AIBN (0.048 g, 0.295 mmol). The mixture was heated at reflux overnight. The reaction mixture was filtered through Celite and the solvent was evaporated. The residue was purified by flash chromatography (hexane:ethyl acetate) to give the desired product (0.98 g, 45.5%) as a light yellow oil. 1H NMR (400 MHz, chloroform-d) δ ppm 8.43-8.51 (m, 1H), 7.84-7.92 (m, 1H), 7.53-7.64 (m, 3H), 7.23-7.34 (m, 3H), 6.50 (d, 1H), 4.50 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304419B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-aedcfd401bbe4b488797dda86d99bc54 |
| Source note | uspto-grants-2012_11 |