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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567133Generated: October 30, 2026

Acetone → HCID 140152, compound

https://huagongshe.com/reaction/567133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant2-MethylbenzaldehydeHCID 10722—
ReactantSodium HydroxideHCID 14798—
ProductHCID 140152HCID 14015286.3%

Reaction Steps

In a 250 ml single neck flask was charged 12.0 g (100 mmoles,1.0 eq) of o-tolualdehyde 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 13.8 g of 4-(o-tolyl)-3-buten-2-one as a faintly yellow oil in 86.3% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177462B1
Source datasetuspto-grants-2001_01
ORD IDord-d5a2ddb29f10452d980b426c3ffaa72c
Source noteuspto-grants-2001_01