HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → Methyl 2-(4-bromomethylphenoxy)-2-(2-chlorophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-(2-chlorophenyl)-2-(4-methylphenoxy)acetate | HCID 19385716 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 2-(4-bromomethylphenoxy)-2-(2-chlorophenyl)acetate | HCID 19385740 | 76.5% |
Reaction Steps
To a solution of 0.200 g (0.69 mmol) of the product of Step C dissolved in 2 mL of carbon tetrachloride was added 0.117 g (0.95 eq) of N-bromosuccinimide and ca. 10 mg (catalytic amount) of AIBN. The reaction mixture was stirred and refluxed under a nitrogen atmosphere for 30 minutes, then cooled and concentrated in vacuo. The residual oil was purified on a silica gel flash chromatography column eluted with 5% ethyl acetate/hexane to afford 0.186 g (73%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05264439 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-11a987a201ed4da6832ce16c6f9f17b1 |
| Source note | uspto-grants-1993_11 |