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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthalenethiol | HCID 7058 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | (3E)-4-Methoxy-3-buten-2-one | HCID 639675 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (E)-4-(2-naphthylthio)-3-buten-2-one | HCID 18795139 | 16.7% |
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
| 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-8599bc832e8d4e51a44a3bf25ff4a4d8 |
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| Source note | uspto-grants-2000_04 |
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