HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → Methyl-7-cyclopentyloxy-2-bromomethylbenzo[b]furan-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl-7-cyclopentyloxy-2-methylbenzo[b]furan-4-carboxylate | HCID 44247883 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl-7-cyclopentyloxy-2-bromomethylbenzo[b]furan-4-carboxylate | HCID 66592560 | 5.8% |
Reaction Steps
To a well stirred refluxing solution of AIBN (500 mg) and N-bromosuccinimide (30.5 g, 0.171 moles) in carbon tetrachloride (500 mL) was added a Methyl-7-cyclopentyloxy-2-methylbenzo[b]furan-4-carboxylate (43.0 g, 0.151 moles) and refluxed for 2-3 hours. Reaction mixture was cooled to room temperature and filtered thorough Celite bed. The filtrate was concentrated under vacuo to give product (3.1 g) as brown oil. The product obtained (50.0 g) was taken ahead for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943634B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-de4918fa7718476bbf6bb68083e39d28 |
| Source note | uspto-grants-2011_05 |