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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395211Generated: October 25, 2026

Acetic Acid → 2-Methyl-3-[4-(2-methylbutan-2-yl)phenyl]prop-2-enal

https://huagongshe.com/reaction/1395211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPropanalHCID 527—
ReactantPotassium HydroxideHCID 14797—
Reactant4-(2-Methylbutan-2-yl)benzaldehydeHCID 473780—
SolventMethanolHCID 887—
Product2-Methyl-3-[4-(2-methylbutan-2-yl)phenyl]prop-2-enalHCID 53395197—

Reaction Conditions

Temperature40 °C

Reaction Steps

162.2 g of p-tert.amyl-benzaldehyde are added under nitrogen gasification to a solution of 1.56 g of potassium hydroxide in 113 ml of methanol and 48.8 g of propionaldehyde are subsequently added dropwise at 40° C. over a period of 6 hours. The mixture is subsequently stirred at 40° C. for an additional hour, 2 ml of acetic acid are added and the mixture is concentrated on a rotary evaporator. The oily suspension is taken up in ether, washed neutral with water, dried and evaporated. By distillation there is obtained pure 3-(p-tert.amyl-phenyl)-2-methyl-acrolein of boiling point 117°-120° C./0.035 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04202894
Source datasetuspto-grants-1980_05
ORD IDord-c926f46e5f784b86b3a6303201b42868
Source noteuspto-grants-1980_05