HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14207Erstellt: 24. Oktober 2026
m-Chloroperbenzoic acid → Methyl 6-methylnicotinate 1-oxide
https://huagongshe.com/de/reaction/14207
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Edukt | Methyl 6-methylnicotinate | HCID 231548 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Methyl 6-methylnicotinate 1-oxide | HCID 15883477 | 92,8% |
Reaktionsschritte
To a solution of methyl 6-methylnicotinate (6.05 g) in methylene chloride (100 mL) was added m-chloroperbenzoic acid (77%, 13.5 g). The reaction mixture was stirred at room temperature for 2 h and then diluted with chloroform (100 mL). The mixture was washed successively with aqueous sodium sulfite, saturated sodium bicarbonate, and brine. The organic later was then dried (sodium sulfate), filtered, and concentrated under reduced pressure to provide 6.21 g of methyl 6-methylnicotinate 1-oxide. A solution of methyl 6-methylnicotinate 1-oxide (4.35 g) in acetic anhydride (50 mL) was heated at 120° C. for 2 h and then concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 1:2 to 3:5 ethyl acetate/hexanes) provided 3.3 g of the title compound: 3H NMR (300 MHz, CDCl3) δ 9.18, 8.31, 7.44, 5.29, 3.96, 2.19.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07727997B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-40dc59b8757c438b9eb3b2a6028290ff |
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| Quellennotiz | uspto-grants-2010_06 |
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