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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantSodium BicarbonateHCID 516892—
Reactant(3E)-4-Methoxy-3-buten-2-oneHCID 639675—
SolventBenzeneHCID 241—
Product4-(Phenylsulfanyl)but-3-en-2-oneHCID 6269152—

Reaction Conditions

Temperature55 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06049009
Source datasetuspto-grants-2000_04
ORD IDord-280fc3a25aeb4ca6ab03b6a3c0115de6
Source noteuspto-grants-2000_04