HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Methyl-2-bromomethyl-7-methoxybenzo[b]furan-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl-7-methoxy-2-methylbenzo[b]furan-4-carboxylate | HCID 66592954 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl-2-bromomethyl-7-methoxybenzo[b]furan-4-carboxylate | HCID 66592982 | 57.1% |
Reaction Steps
To a well stirred refluxing solution of AIBN (40.0 mg, 1.0%) and N-bromo succinimide (3.4 g, 19.05 mmol) in carbon tetrachloride (60.0 mL) was added a Methyl-7-methoxy-2-methylbenzo[b]furan-4-carboxylate (from step 5) (4.0 g, 18.16 mmol) 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 was taken ahead for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129401B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-69e76ed3c8cf40b6a3bc5056c99aae78 |
| Source note | uspto-grants-2012_03 |