HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Bromo-7-(4-methylbenzyl)-1-benzothiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-(4-Methylbenzyl)benzo[b]thiophene | HCID 67069100 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Bromo-7-(4-methylbenzyl)-1-benzothiophene | HCID 67069091 | 56% |
Reaction Steps
An acetonitrile (30 mL) solution of 7-(4-methylbenzyl)-1-benzothiophene (1.24 g, 5.20 mmol) was added with N-bromosuccinimide (1.01 g, 5.72 mmol) and stirred at room temperature for two hours. The solvent was evaporated under reduced pressure and diluted with ethyl acetate. After washed with 20 wt % sodium thiosulfate aqueous solution and brine, the organic phase was dried with anhydrous magnesium sulfate. After the desiccant was filtered off, the residue obtained by evaporating the solvent under reduced pressure was purified by silica gel column chromatography (hexane:ethyl acetate=100:1-50:1) to obtain a colorless powdered title compound (0.92 g, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910619B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-f48401b91bce46a7bb139f0115a9f2ae |
| Source note | uspto-grants-2011_03 |