HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Bis(adamantan-1-yl)(butyl)phosphane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Di-1-adamantylphosphine | HCID 11077518 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Butyl ether | HCID 8909 | — |
| Product | Bis(adamantan-1-yl)(butyl)phosphane | HCID 11371790 | — |
Reaction Steps
4.6 g (15 mmol) of di(1-adamantyl)phosphine were placed in 50 ml of di-n-butyl ether, and 20 ml of a 2.5 M solution of n-BuLi in toluene (50 mmol) were added. The mixture was refluxed for 1 h and cooled and 4.1 g (30 mmol) of 1-butyl bromide were added dropwise. The mixture was refluxed for 30 min, cooled and washed with saturated ammonium chloride solution (3×), the organic phase was separated off and dried over sodium sulfate and the solvent was distilled off under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148176B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-5940c09a5928463c9261bc1c3cda896e |
| Source note | uspto-grants-2006_12 |