HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Tetra-n-butylphosphonium Diphenylphosphinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diphenylphosphinic acid | HCID 15567 | — |
| Catalyst | Tetrabutylphosphonium chloride | HCID 75311 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tetra-n-butylphosphonium Diphenylphosphinate | HCID 21328170 | — |
Reaction Steps
To a suspension of 43.6 grams of diphenylphosphinic acid in 300 milliliters of distilled water is added a solution of 8.0 grams of sodium hydroxide in 200 milliliters of water and the mixture stirred. The acid dissolves slowly. To the resulting solution is added a solution of 59 grams of tetra-n-butylphosphonium chloride in about 200 milliliters of distilled water. The reaction mixture is stirred for half an hour and is then extracted with about 500-milliliter portion of chloroform. The extract is dried over anhydrous Na2SO4 and the chloroform is then distilled. A light-brown viscous liquid remains. It is dried overnight at 80° C. On cooling, tetra-n-butylphosphonium diphenylphosphinate separates as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04145473 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-273dc3e8c39646b89cee53365222f12e |
| Source note | uspto-grants-1979_03 |