Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Butyl bromide | HCID 8002 | — |
| Edukt | Trioctylphosphine | HCID 20851 | — |
| Produkt | Tri-n-octyl-n-butylphosphonium bromide | HCID 22731140 | — |
Reaktionsschritte
Tri-n-octyl-n-butylphosphonium bromide is prepared by slowing dripping tri-(n-octyl)phosphine (740 grams) into refluxing 1-bromobutane (500 grams) in a nitrogen atmosphere. Reflux is continued 1 hour after final addition then the solution is cooled with stirring for about 18 hours, followed by vacuum removal of excess 1-bromobutane at 60° C. This product, 1210 grams from two successive preparations, is added to 880 grams of sodium 3,5-dicarbomethoxybenzenesulfonate in 2500 ml. of water and stirred for at least 1 hour at 85° C. then the heat is removed and the oil-in-water mixture is stirred for about 18 hours. The oil layer is separated from the water, rinsed with 1000 ml. of water and dried at about 80° C. at a pressure less than 2 torr for 18 hours. This product, an oil, is tri-n-octyl-n-butylphosphonium 3,5-dicarbomethoxybenzenesulfonate with 4.2% phosphorous and 4.7% sulfur by analysis.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04006123 |
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| Quelldatensatz | uspto-grants-1977_02 |
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| ORD ID | ord-c2c4bc6bda874a5fb100a3f0c34794ee |
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| Quellennotiz | uspto-grants-1977_02 |
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