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HRID 5666Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/5666

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktOxalic AcidHCID 971—
EduktDiisobutylaluminumhydrideHCID 21225700—
Edukt2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 53657145—
LösungsmittelTolueneHCID 1140—
LösungsmittelHexaneHCID 8058—
Produkt2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenalHCID 5444191884%

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

To a solution of 2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile (856 mg, 3.0 mmol) in n-hexane (30 ml) was added a 0.5 M solution of diisobutylaluminium hydride in toluene (6 ml) with stirring at -70° C. under argon atmosphere. After one hour, water (3 ml) was added, the cooling bath was removed, and the reaction mixture was stirred well. Resultant white precipitates were filtered and washed. The filtrate was concentrated to give a residue, which was dissolved in n-hexane (10 ml). The n-hexane solution was combined with a 10% aqueous solution of oxalic acid (5 ml) and stirred for 3 hours. The organic layer was extracted and separated, washed with water, dried over MgSO4, and concentrated. The resultant residue was subjected to silica gel column chromatography (solvent: n-hexane/ethyl acetate=10:1) to obtain 2 -(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenal (865 mg, 84%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05245085
Quelldatensatzuspto-grants-1993_09
ORD IDord-1beec0472a4d456a82991908e309a084
Quellennotizuspto-grants-1993_09