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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(2-Methylbutan-2-yl)benzaldehyde | HCID 473780 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Methyl-3-[4-(2-methylbutan-2-yl)phenyl]prop-2-enal | HCID 53395197 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04202894 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-c926f46e5f784b86b3a6303201b42868 |
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| Source note | uspto-grants-1980_05 |
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