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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004493Generated: October 25, 2026

2-Naphthalenethiol → (E)-4-(2-naphthylthio)-3-buten-2-one

https://huagongshe.com/reaction/1004493

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphthalenethiolHCID 7058—
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant(3E)-4-Methoxy-3-buten-2-oneHCID 639675—
SolventBenzeneHCID 241—
Product(E)-4-(2-naphthylthio)-3-buten-2-oneHCID 1879513916.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of (E)-4-methoxy-3-buten-2-one (purity: 90%, 15.0 ml, 0.13 mol) and 2-naphthalenethiol (21.16 g, 0.13 mol) in benzene (180 ml) was added p-toluene sulfonic acid-monohydrate (75 mg, 0.4 mmol), followed by heating, while stirring, on an oil bath at 50° C. for 70 minutes. After ice cooling, an aqueous saturated sodium hydrogen carbonate solution was added thereto, followed by extracting with ethyl acetate four times. The ethyl acetate layer was washed with an aqueous saturated sodium hydrogen carbonate solution and saturated brine twice and then dried with anhydrous magnesium sulfate. After concentrating under a reduced pressure, the residue was treated with the column chromatography (670 g, n-hexane:methylene chloride:ethyl acetate=1:0:0-1:3:0-2:0:1), followed by recrystallizing from n-hexane-ethyl ether to thereby obtain the titled compound as a light brown crystalline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06049009
Source datasetuspto-grants-2000_04
ORD IDord-8599bc832e8d4e51a44a3bf25ff4a4d8
Source noteuspto-grants-2000_04