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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639886Generated: October 26, 2026

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

https://huagongshe.com/reaction/1639886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant(2E)-3-(2,6-dimethoxyphenyl)acrylonitrileHCID 59658521—
SolventTolueneHCID 1140—
Product(2E)-3-(2,6-dimethoxyphenyl)acrylaldehydeHCID 2392819360%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110579B2
Source datasetuspto-grants-2012_02
ORD IDord-2a7a4a683f794601ba19e02d7dc64023
Source noteuspto-grants-2012_02