HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 259387Erstellt: 24. Oktober 2026
Sodium Hydroxide → Tetra-n-butylphosphonium Diphenylphosphinate
https://huagongshe.com/de/reaction/259387
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Diphenylphosphinic acid | HCID 15567 | — |
| Katalysator | Tetrabutylphosphonium chloride | HCID 75311 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Tetra-n-butylphosphonium Diphenylphosphinate | HCID 21328170 | — |
Reaktionsschritte
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 two 250-milliliter portions 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. It is collected by filtration and is washed with anhydrous ether; the crystals melt at 83° to 84° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04038258 |
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| Quelldatensatz | uspto-grants-1977_07 |
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| ORD ID | ord-78e0b9d63bd54bd38eb65dd5567686b6 |
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| Quellennotiz | uspto-grants-1977_07 |
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