HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 1H-Indole, 5-bromo-3-(2-bromoethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-Bromo-1H-indole-3-ethanol | HCID 122956 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1H-Indole, 5-bromo-3-(2-bromoethyl)- | HCID 18399706 | — |
Reaction Steps
A solution of 11.5 g of triphenylphosphine in 60 ml of dichloromethane is added to a solution, cooled to 0° C., of 4 g of the compound obtained in Step 1 and 7.5 g of carbon tetrabromide in 100 ml of dichloromethane. After stirring for 48 hours at ambient temperature, the reaction mixture is concentrated in vacuo. The residue obtained is chromatographed on silica gel (dichloromethane/cyclohexane: 80/20), enabling the expected product to be isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399616B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-490ad3aae54f4bef8d6f7d1f68fa186d |
| Source note | uspto-grants-2002_06 |