HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004492Generated: October 25, 2026
Thiophenol → 4-(Phenylsulfanyl)but-3-en-2-one
https://huagongshe.com/reaction/1004492
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (3E)-4-Methoxy-3-buten-2-one | HCID 639675 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-(Phenylsulfanyl)but-3-en-2-one | HCID 6269152 | — |
Reaction Steps
To a solution of (E)-4-methoxy-3-buten-2-one (purity 90%, 5.66 ml, 49.9 mmol) and thiophenol (5.13 ml, 49.9 mmol) in benzene (60 ml) was added p-toluene 25 sulfonic acid-monohydrate (30 mg, 0.16 mmol), followed by heating while stirring on an oil bath at 55° C. for 30 minutes. After ice cooling, an aqueous saturated sodium hydrogen carbonate solution was added thereto, followed by extracting with cyclohexane 3 times. The organic layer was washed with an aqueous saturated sodium hydrogen carbonate solution twice and with saturated brine, followed by drying with anhydrous magnesium sulfate. After concentrating under a reduced pressure, the residue was treated with the column chromatography (190 g, n-hexane:ethyl acetate=10:1). After evaporated under a reduced pressure, the titled compound was recrystallized from n-hexane-n-nonane to obtain as a colorless crystalline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06049009 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-280fc3a25aeb4ca6ab03b6a3c0115de6 |
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| Source note | uspto-grants-2000_04 |
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