HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248068Generated: October 30, 2026
Acetone → 1,5-Bis[4-(trifluoromethyl)phenyl]penta-1,4-dien-3-one
https://huagongshe.com/reaction/1248068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Trifluoromethyl)benzaldehyde | HCID 67996 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 1,5-Bis[4-(trifluoromethyl)phenyl]penta-1,4-dien-3-one | HCID 592241 | 74.6% |
Reaction Steps
A solution of sodium hydroxide (15 g of 10% aqueous) is added with stirring, and under a nitrogen atmosphere to a solution of 4-trifluoromethylbenzaldehyde (6.42 g; 0.369 mol) in heptane (70 ml). Next, a solution of acetone (10.7 g; 0.184 mol) in heptane (30 ml) is added to the above two phase system at a temperature range of from 25° C. to 30° C. over a period of two hours. The reaction mixture is then stirred for two hours at 25° C. to 30° C. Concentrated hydrochloric acid (9.4 ml) and isopropyl alcohol (48 ml) are then added, the mixture heated at reflux for 1.5 hours, and is then cooled to 20° C. The precipitated solid is filtered, washed with heptane (40 ml), and water and dried under vacuum to afford 50.8 g of title product, 98.8% pure, mp 154° C. to 156° C. (yield: 73.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04521629 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-2312fb2aa5914a529f67b9146ca10b3b |
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| Source note | uspto-grants-1985_06 |
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