HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77663Generated: October 26, 2026
Acetone → 1,5-Bis(3-methylphenyl)-1,4-pentadien-3-one
https://huagongshe.com/reaction/77663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Methylbenzaldehyde | HCID 12105 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,5-Bis(3-methylphenyl)-1,4-pentadien-3-one | HCID 3456218 | 72% |
Reaction Steps
3-Methylbenzaldehyde (1ab, 3.00 ml, 25.4 mmol) and acetone (19, 0.94 ml, 12.7 mmol) were combined in ethanol (20 ml) and stirred for 15 min at room temperature. A solution of sodium hydroxide (1.50 g, 37.5 mmol) and water (20 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting mixture was extracted into ethyl acetate, washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to afford a solid. The crude solid was recrystallized from ethanol to give 2.39 g (72%) of a yellow solid: mp 68-72° C. [expected mp 68-72° C.]; 1H NMR: δ 2.38 (s, 6H), 7.06 (d, 2H, J=15.9 Hz), 7.26 (m, 4H), 7.40 (m, 4H), 7.70 (d, 2H, J=15.9 Hz); 13C NMR: δ 21.3, 125.1, 125.4, 128.6, 128.8, 131.1, 134.6, 138.4, 143.1, 188.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841326B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-5092852dab894a7c83a10adce66f037a |
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| Source note | uspto-grants-2014_09 |
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