Reaktionsgleichung
[P:1]([Cl:4])(Cl)Cl.[CH2:5]([NH:7][CH2:8][CH3:9])[CH3:6]>C(OCC)C>[Cl:4][P:1]([N:7]([CH2:8][CH3:9])[CH2:5][CH3:6])[N:7]([CH2:8][CH3:9])[CH2:5][CH3:6]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of phosphorous trichloride (26 ml; 0.298 mol) in dry diethylether (500 ml) at −78° C., acetone/CO2 bath, under dry nitrogen gas atmosphere was added diethylamine (123.4 ml; 1.19 mol) dropwise via a pressure equalised dropping funnel over 2 hrs. A thick suspension formed, reaction allowed to warm to ambient temperature and stirred for an additional 2 hrs. After this time the suspension was filtered under dry nitrogen gas via an oven dried filter stick, washing with dry diethylether (3×100 ml). Filtrate was evaporated under high vacuum on the Schlenk line, using a cold-finger trap to condense solvent vapours, to give an oil. The oil was purified by distillation under reduced pressure to give the required product (b.p. 105° C. @ 10 mmHg; 49 g; 70% yield). 1H NMR (300 MHz, CDCl3), δ/ppm; 1.08 (6H, t J=7.0, CH3), 3.08 (4H, ap. br. d J=7.0, CH2); 31P NMR (121 MHz, CDCl3) δ/ppm; 159.9.
Aufarbeitung
- customover 2 hrs
- customA thick suspension formed
- customreaction
- filtrationAfter this time the suspension was filtered under dry nitrogen gas via an oven
- customdried
- filtrationfilter stick
- washwashing with dry diethylether (3×100 ml)
- customFiltrate was evaporated under high vacuum on the Schlenk line
- customto condense solvent vapours
- customto give an oil
- distillationThe oil was purified by distillation under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-266d3613137d4784a0499e0f4ff1de57
- Quelldatensatz
- uspto-grants-2011_11
- Patentnummer
- US08067642B2
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