HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369824Generated: October 31, 2026
Acetone → 4-(4-Hydroxy-3-methoxyphenyl)-3-buten-2-one
https://huagongshe.com/reaction/2369824
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Hydroxy-3-methoxyphenyl)-3-buten-2-one | HCID 14121 | 87.1% |
Reaction Steps
To a solution of acetone (15.30 g, 263.76 mmol) in a mixture of ethanol (35 mL) and water (15 mL) were added sodium hydroxide (2.90 g, 72.54 mmol) and 4-hydroxy-3-methoxybenzaldehyde (5.01 g, 32.97 mmol). The reaction mixture was stirred at room temperature for 15 h. The reaction was cooled to 0° C. and quenched with 2.0 N hydrochloric acid until the solution became slightly acidic. The solution was extracted with ethyl acetate (4×100 mL). The combined organic layers were washed with water (50 mL) and saturated aqueous sodium chloride (50 mL). The organic layer was dried over magnesium sulfate, filtered, and concentrated at reduced pressure to afford 4-(4-hydroxy-3-methoxy-phenyl)but-3-ene-2-one (5.52 g, 87% yield) as a yellow solid: MS (EI) for C11H12O3: 193 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710038B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-2782a4bd50764bc98b229d7c3e9ac000 |
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| Source note | uspto-grants-2014_04 |
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