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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221848Generated: October 27, 2026

Sulfuric Acid → 1-(4-Methoxyphenyl)butane-1,3-dione

https://huagongshe.com/reaction/221848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant4'-MethoxyacetophenoneHCID 7476—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
CatalystEthanolHCID 702—
Catalyst18-Crown-6HCID 28557—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Methoxyphenyl)butane-1,3-dioneHCID 7764060.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 9.80 mL of ethyl acetate (100 mmol) in 40 mL dry THF at room temperature was added 2.0 g of 60% sodium hydride (49.9 mmol), 7.50 g of 4′-methoxyacetophenone (49.9 mmol), 100.0 mg of 18-crown-6 (0.40 mmol), and 2 drops of ethanol. After 30 minutes, the reaction was refluxed for 1 h, and then 100 mL of dry THF was added. After an additional 1 h, 30 mL THF was added. After 1 h the reaction was cooled to 0° C. and 25 mL of 10% aqueous sulfuric acid was added. The product was extracted with diethyl ether. The ether extracts were dried with Na2SO4, filtered, and concentrated in vacuo. The crude material was purified via silica gel chromatography eluting with 4:1 hexane:ethyl acetate to give 5.8 g of 1-(4-methoxyphenyl)butane-1,3-dione containing 30% starting material (via 1H NMR 42% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207168B2
Source datasetuspto-grants-2012_06
ORD IDord-8c7ebcd2583645af97db7647fa4bff5c
Source noteuspto-grants-2012_06