Triphenylphosphine → HCID 13232911, Verbindung

Temperatur

10 °C

Undecyltriphenylphosphonium bromide (16.3 g, prepared by heating 1-bromoundecane and triphenylphosphine together in refluxing xylene) is suspended in dry ether (400 ml) and the mixture is stirred under nitrogen whilst 1.7 M butyllithium in hexane (47.5 ml) is added from a syringe. The resulting bright red solution is cooled to 10° C. and treated dropwise with ethyl 5-oxopentanoate (7.25 g) in dry ether (50 ml). After 10 minutes, water (200 ml) is added and when the solid product has dissolved the ether layer is separated and the aqueous layer is washed with ether (3×100 ml). The combined ethereal solutions are dried over magnesium sulphate and the ether is evaporated. The residue is shaken with hexane (200 ml), and the mixture is cooled and filtered. The filtrate is concentrated to a volume of 100 ml and then cooled to allow crystallisation of the triphenylphosphine oxide. When this is complete, the mixture is filtered and the filtrate is evaporated to yield ethyl (Z)-hexadec-5-enoate in crude form as a yellow oil (10.1 g).

1. additionis added from a syringe
2. customis separated
3. washthe aqueous layer is washed with ether (3×100 ml)
4. dry with materialThe combined ethereal solutions are dried over magnesium sulphate
5. customthe ether is evaporated
6. temperaturethe mixture is cooled
7. filtrationfiltered
8. concentrationThe filtrate is concentrated to a volume of 100 ml
9. temperaturecooled
10. customcrystallisation of the triphenylphosphine oxide
11. filtrationWhen this is complete, the mixture is filtered
12. customthe filtrate is evaporated

ORD-Eintrag

ord-8a878d2b4a0c47389c92b3018afb300a

Quelldatensatz

uspto-grants-1989_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04844892