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HRID 5665Erstellt: 23. Oktober 2026

Water → 2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile

https://huagongshe.com/de/reaction/5665

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukta FarnesolHCID 3327—
EduktPotassium bis(trimethylsilyl)amideHCID 3251421—
EduktPhosphonic acid, (1-cyano-2-methylpropyl)-, diethyl esterHCID 11031342—
LösungsmittelTolueneHCID 1140—
Produkt2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 5365714596%

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

To a solution of 2-(diethylphosphono)isovaleronitrile (8.72 g, 40 mmol) in toluene (75 ml) was gradually added a 0.5 M solution of potassium bis(trimethylsilyl)amide in toluene (75 ml) with stirring at -70° C. under argon atmosphere. The cooling bath was removed, and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was cooled to -70° C. again, and farnesol (5.88 g, 26.7 mmol) was added thereto with stirring, and the mixture was allowed to warm to room temperature. After addition of water, the organic layer was separated, washed with saturated aqueous sodium bicarbonate and then saturated aqueous sodium chloride, and dried over MgSO4. The organic layer was separated from MgSO4 by filtration and concentrated to give a residue, which was purified with silica gel column chromatography (solvent: n-hexane/ethyl acetate=100:1) to obtain the aimed 2 -(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile (7.23 g, 96%; 2Z:2E=25.6:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05245085
Quelldatensatzuspto-grants-1993_09
ORD IDord-d891efc28e36422aa4bc843ada73ddc3
Quellennotizuspto-grants-1993_09