Sodium borohydride → Tris(pentafluoroethyl)phosphane
Reaktionsgleichung
F[P:2](F)([C:17]([F:23])([F:22])[C:18]([F:21])([F:20])[F:19])([C:10]([F:16])([F:15])[C:11]([F:14])([F:13])[F:12])[C:3]([F:9])([F:8])[C:4]([F:7])([F:6])[F:5].[BH4-].[Na+]>>[F:9][C:3]([P:2]([C:10]([F:15])([F:16])[C:11]([F:12])([F:13])[F:14])[C:17]([F:23])([F:22])[C:18]([F:21])([F:20])[F:19])([F:8])[C:4]([F:7])([F:6])[F:5]Komponenten
Reaktionsbedingungen
- Temperatur
- 110 °C
Versuchsvorschrift
230.0 g (0.54 mol) of difluorotris(pentafluoroethyl)phosphorane and 41.2 g (1.089 mol) of sodium borohydride were refluxed with vigorous stirring for 3 hours in a glass flask at a bath temperature of about 110° C. The reaction mixture was subsequently distilled under reduced pressure (2 kPa), and two fractions of the product were collected in cold traps at a temperature of −78° C. and −195° C. respectively. For further purification, the combined products from both traps were distilled under atmospheric pressure under an inert-gas atmosphere, with the fraction in the boiling range 85–87° C. being collected. 194.0 g of pure tris(pentafluoroethyl)phosphine were obtained. The yield was 93%, based on the amount of difluorotris(pentafluoroethyl)phosphorane employed.
Aufarbeitung
- distillationThe reaction mixture was subsequently distilled under reduced pressure (2 kPa), and two fractions of the product
- customwere collected in cold traps at a temperature of −78° C. and −195° C. respectively
- customFor further purification
- distillationthe combined products from both traps were distilled under atmospheric pressure under an inert-gas atmosphere, with the fraction in the boiling range 85–87° C.
- custombeing collected
Quellen und Nachweise
- ORD-Eintrag
- ord-8f0cee2e3b88441099b792c48ae18d42
- Quelldatensatz
- uspto-grants-2007_04
- Patentnummer
- US07208626B2
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