HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 7-(Bromomethyl)-1-benzothiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Methyl-1-benzothiophene | HCID 6428541 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 7-(Bromomethyl)-1-benzothiophene | HCID 10751761 | — |
Reaction Steps
7 g of 7-methylbenzo[b]thiophene, 8,5 g of N-bromosuccinimide and a spatula tip of α,α'-azoisobutyronitrile are refluxed together for 6 hours in 50 ml of carbon tetrachloride. The resulting mixture is cooled, filtered and concentrated by evaporation. The resulting raw title compound can be directly employed in the next step. M.p. when isolated=57° (isopropanol)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04737516 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-b271bc6775614609b28f0c5fa1cee288 |
| Source note | uspto-grants-1988_04 |