HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylamine → 2,2'-Bis((diphenylphosphaneyl)methyl)-1,1'-binaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Dichloroethylsilane | HCID 15706 | — |
| Reactant | 2,2'-Bis(diphenylphosphinylmethyl)-1,1'-binaphthyl | HCID 10952532 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2,2'-Bis((diphenylphosphaneyl)methyl)-1,1'-binaphthalene | HCID 10952407 | — |
Reaction Steps
20.48 g (0.03 mol) of 2,2'-bis(diphenylphosphinylmethyl)-1,1'-binaphthyl are suspended in 80 ml of xylene and 39.3 ml (0.165 mol) of tri-n-butylamine in the absence of air and moisture, and 19.4 g (0.15 mol) of ethyldichlorosilane are added dropwise with stirring. The mixture is then refluxed for 13 hours to give a clear solution. Xylene is distilled off at atmospheric pressure, and the mixture is allowed to cool with stirring. This results in the formation of 2,2'-bis(diphenylphosphinomethyl)-1,1'-binaphthyl as a colorless solid, which is filtered off under an inert gas and washed with 20 ml of degassed acetone. 18.5 g (95%) of colorless crystals of melting point 160° to 161° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05600006 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-be52cbf74f3943c5893a8efee9deda31 |
| Source note | uspto-grants-1997_02 |