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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1040328Erstellt: 25. Oktober 2026

Methanol → (2E)-3-(2,6-dimethoxyphenyl)acrylaldehyde

https://huagongshe.com/reaction/1040328

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktSulfuric AcidHCID 1118—
EduktDiisobutylaluminumhydrideHCID 21225700—
Edukt(2E)-3-(2,6-dimethoxyphenyl)acrylonitrileHCID 59658521—
LösungsmittelTolueneHCID 1140—
Produkt(2E)-3-(2,6-dimethoxyphenyl)acrylaldehydeHCID 2392819360%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Add 355 mL of a 1M solution of diisobutylaluminium hydride (DIBAL-H) (355 mmol) in toluene to a solution of 61 g (322 mmol) of (2E)-3-(2,6-dimethoxyphenyl)acrylonitrile in 600 mL of anhydrous toluene under argon and cooled to 0° C., maintaining the temperature at 0° C. Then bring the reaction mixture to room temperature (RT) and stir for 3 h. Then add 13 mL (322 mmol) of methanol and then, dropwise, 170 g (174 mmol) of an aqueous solution of sulphuric acid at 10 wt. %. Stir the suspension for one hour, then filter on a celite bed. Wash the filtrate with 500 mL of water then dry over Na2SO4 and concentrate under reduced pressure. Take up the residue obtained in 500 mL of DCM and filter in a silica column, eluting with DCM. After concentration under reduced pressure, we obtain 37 g of (2E)-3-(2,6-dimethoxyphenyl)acrylaldehyde in the form of colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08552201B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-088b344ef0ad49559dc9a20036affd12
Quellennotizuspto-grants-2013_10