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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Phenyl-4-sulfanylidenebutan-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04622322 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-19df323271604851b54e0eb740658708 |
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| Source note | uspto-grants-1986_11 |
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