HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 2-(2,2-Dibromo-vinyl)benzo[b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Benzothiophene-2-carbaldehyde | HCID 736500 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2,2-Dibromo-vinyl)benzo[b]thiophene | HCID 86599047 | 67% |
Reaction Steps
A solution of benzo[b]thiophene-2-carbaldehyde (1.0 g, 6.17 mmol) and carbon tetrabromide (3.1 g, 9.25 mmol) in methylene chloride (50 mL) was cooled to 0° C. A solution of triphenylphosphine (4.86 g, 18.3 mmol) in methylene chloride (20 mL) was added dropwise. After ½ hour the solution was placed on a plug of silica gel and eluted with 20% ethyl acetate:hexane. Concentration of the eluent resulted in the isolation of 1.3 g (67%) of 2-(2,2-Dibromo-vinyl)-benzo[b]thiophene as a yellow oil, which was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07419980B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-fb46d5b5b06c4737a6d4c7248eadfe0a |
| Source note | uspto-grants-2008_09 |