HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733271Generated: October 26, 2026
Acetic Acid → 2-Propenal, 3-[4-(1,1-dimethylethyl)phenyl]-2-methyl-
https://huagongshe.com/reaction/1733271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Propanal | HCID 527 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Propenal, 3-[4-(1,1-dimethylethyl)phenyl]-2-methyl- | HCID 114659 | — |
Reaction Steps
108.5 g of p-tert.butyl-benzaldehyde are added under nitrogen gasification to a solution of 1.4 g of potassium hydroxide in 100 ml of methanol and 39.2 g of propionaldehyde are subsequently added dropwise at 40° C. over a period of 6 hours. Subsequently, the mixture is further stirred at 40° C. for 1 hour, 1.5 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.butyl-phenyl)-2-methyl-acrolein of boiling point 165° C./11 Torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04241058 |
|---|
| Source dataset | uspto-grants-1980_12 |
|---|
| ORD ID | ord-7ba3d7c254654ce5a4ed8c6e78790a40 |
|---|
| Source note | uspto-grants-1980_12 |
|---|