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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731548Generated: November 1, 2026

Ethanol → 4-Phenyl-4-sulfanylidenebutan-2-one

https://huagongshe.com/reaction/1731548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPhenacyl bromideHCID 6259—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178418634HCID 178418634—
SolventDiethyl EtherHCID 3283—
Product4-Phenyl-4-sulfanylidenebutan-2-oneHCID 23356053—

Reaction Steps

To a solution of 54.0 g (1.0M) sodium methoxide in 100 ml absolute ethanol stirring under nitrogen at reflux temperature 74 ml (76.1 g, 1.0M) thioacetic acid is added dropwise over a period of 0.5 hours. Upon complete addition the solution is refluxed for 15 minutes. To the yellow solution stirring under nitrogen atmosphere at reflux temperature, a solution of 199.1 g (1.0M) α-bromoacetophenone in 800 ml absolute ethanol is added rapidly dropwise over a period of 70 minutes. After complete addition, the suspension formed is refluxed for 3 hours. The reaction mixture is cooled and the precipitated NaBr is removed by vacuum filtration. The filtrate is concentrated in vacuo to give a brown oil with some solid present. This mixture is suspended in 500 ml of ether and is filtered to remove insoluble NaBr. The filtrate is stirred with activated charcoal for 0.5 hours, filtered, and concentrated in vacuo to give a red-brown oil. This oil is purified by vacuum distillation and the fraction is collected at 133°-137°/0.2-0.05 mm Hg and characterized by NMR as α-acetylthioacetophenone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04622322
Source datasetuspto-grants-1986_11
ORD IDord-19df323271604851b54e0eb740658708
Source noteuspto-grants-1986_11