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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567131Generated: October 25, 2026

Acetone → o-Anisalacetone

https://huagongshe.com/reaction/567131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
Reactant2-MethoxybenzaldehydeHCID 8658—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Producto-AnisalacetoneHCID 13918182.3%

Reaction Steps

In a 250 ml single neck flask was charged 13.6 g (100 mmoles,1.0 eq) of o-methoxybenzaldehyde dissolved in 30 ml of acetone. To this was added 5 g of 10% aqueous sodium hydroxide solution (12.5 mmoles, 0.125 eq), dropwise and during the course of addition, temperature was kept no higher than 25° C., while the mixture was agitated continuously for 30 minutes. To the mixture was added 50 ml of water, followed by 100 ml of ethyl acetate, the phases were separated and the organic phase was washed with water three times and then dried, and concentrated to obtain 14.5 g of 4-(2-methoxyphenyl)-3-buten-2-one as a faintly yellow oil in 82.3% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177462B1
Source datasetuspto-grants-2001_01
ORD IDord-621265a941cc4a0f82c157dd4ce3f47b
Source noteuspto-grants-2001_01