HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexane → 3-(3-bromopropyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Triphenylphosphine dibromide | HCID 70579 | — |
| Reactant | Indole-3-propanol | HCID 77115 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(3-bromopropyl)-1H-indole | HCID 10037192 | 99.4% |
Reaction Steps
To a solution of 2 g (11.41 mmol) of 3-(1H-indol-3-yl)propanol in 40 ml of dioxane was added at room temperature 5.3 g (12.55 mmol) of dibromotriphenylphosphorane and the resulting solution was stirred during 18 h. An excess of cyclohexane was added and the resulting precipitate was filtered and discarded. The solvent was evaporated to dryness to give 2.7 g (99%) of product as an oil which was used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06974819B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-eeb14de8206a4951914cf43bcae514b2 |
| Source note | uspto-grants-2005_12 |