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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantVanillinHCID 1183—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-(4-Hydroxy-3-methoxyphenyl)-3-buten-2-oneHCID 1412187.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710038B2
Source datasetuspto-grants-2014_04
ORD IDord-2782a4bd50764bc98b229d7c3e9ac000
Source noteuspto-grants-2014_04