Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1389181Erstellt: 25. Oktober 2026

Water → 2-Oxo-5-phenoxypentylidenetriphenylphosphorane

https://huagongshe.com/reaction/1389181

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-(Triphenylphosphoranylidene)acetoneHCID 15038—
EduktBenzene, (2-bromoethoxy)-HCID 68526—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
LösungsmittelChloroform-DHCID 71583—
Produkt2-Oxo-5-phenoxypentylidenetriphenylphosphoraneHCID 2029855145,6%

Reaktionsbedingungen

Temperatur-65 °C

Reaktionsschritte

A solution of n-butyl lithium (2.69 g) in hexane (26.25 ml) was added dropwise to a stirred solution of 2-oxopropylidenetriphenylphosphorane (12.73 g) in anhydrous tetrahydrofuran (400 ml) at -65° C. in an atmosphere of dry nitrogen. The red solution was stirred at -65° C. for a further 15 minutes and was then treated with a solution of 2-phenoxyethyl bromide (8.04 g) in anhydrous tetrahydrofuran (40 ml). The mixture was stirred at 0° C. for one hour and then at ambient temperature for 2 hours, and was poured into water and extracted with diethyl ether. The organic solution was washed with water then dried over magnesium sulphate. Evaporation of the solution gave a yellow gum which slowly hardened on prolonged storage after trituration with diethyl ether to give crude 2-oxo-5-phenoxypentylidenetriphenylphosphorane (8.0 g), m.p. 83°-89° C. [elemental analysis: P, 7.4%; C29H27O2P requires P, 7.1%. νmax 715, 755, 1110, 1400, 1445, 1490 and 1555 cm-1. NMR (approximately 10% w/v solution in deuterochloroform): multiplets at 6.7-7.9δ and 1.8-2.7δ, triplet at 4.0δ (J=6 cycles/second)].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04243683
Quelldatensatzuspto-grants-1981_01
ORD IDord-e6fe9ce61f554ec7a6551492dbfe4684
Quellennotizuspto-grants-1981_01