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HRID 280200Erstellt: 25. Oktober 2026
m-Chloroperbenzoic acid → 2H-Pyrano(2,3-b)pyridine, 2-(3,4-dichlorophenyl)-3,4-dihydro-6-(methylsulfinyl)-
https://huagongshe.com/reaction/280200
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Edukt | 2-(3,4-Dichlorophenyl)-3,4-dihydro-6-(methylthio)-2h-pyrano[2,3-b]pyridine | HCID 514906 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2H-Pyrano(2,3-b)pyridine, 2-(3,4-dichlorophenyl)-3,4-dihydro-6-(methylsulfinyl)- | HCID 514902 | — |
Reaktionsschritte
To a stirred solution of 1.0 g of 2-(3,4-dichlorophenyl)-3,4-dihydro-6-(methylthio)-2H-pyrano[2,3-b]pyridine in 25 ml of methylene chloride at -25° C. there was added dropwise a solution of 0.55 g of 80-85% m-chloroperoxybenzoic acid in 20 ml of methylene chloride over 5-10 minutes while keeping the temperature between -20° and -30° C. A precipitate formed. The mixture was then allowed to warm to -5° C. over 2 hours and then extracted with aqueous saturated sodium bicarbonate solution, aqueous saturated sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure to leave a pale yellow solid. This was recrystallized from a mixture of ethyl acetate and hexane to give 2-(3,4-dichlorophenyl)-3,4-dihydro-6-(methylsulfinyl)-2H-pyrano[2,3-b]pyridine as a cream-colored solid melting at about 159°-162° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04588733 |
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| Quelldatensatz | uspto-grants-1986_05 |
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| ORD ID | ord-82478400a44a4653986ff8d0fe8f1ed6 |
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| Quellennotiz | uspto-grants-1986_05 |
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