HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280809Erstellt: 25. Oktober 2026
2-Hexanol → N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(1-methylpentyloxycarbonyl)benzenesulfonamide
https://huagongshe.com/reaction/280809
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Hexanol | HCID 12297 | — |
| Edukt | Metsulfuron-methyl | HCID 52999 | — |
| Edukt | Trimethylaluminum | HCID 16682925 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-(1-methylpentyloxycarbonyl)benzenesulfonamide | HCID 13176699 | 57,8% |
Reaktionsschritte
2-Hexanol (0.61 g) in 2 ml dry toluene was slowly added at room temperature to a solution of 1.5 ml (2M) trimethylaluminum diluted with 5.0 ml dry toluene under nitrogen. The mixture was stirred at room temperature for 15 minutes and 0.95 g of N-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)aminocarbonyl]-2-methoxycarbonylbenzenesulfonamide was added. The mixture was warmed under N2 to reflux temperature for 2.5 hr. cooled to room temperature and carefully quenched with 20 ml 10% HCl. The organic phase was taken up in methylene chloride, separated, washed with water, dried over magnesium sulfate, filtered and the solvent evaporated under reduced pressure to give 0.65 g of the desired compound which melted at 125°-130° C. The infrared spectrum exhibited characteristic absorption for the product at 3300, 1725, 1730, 1585, 1555 cm-1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04591378 |
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| Quelldatensatz | uspto-grants-1986_05 |
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| ORD ID | ord-1b6f84f99896488e91b94ac211d2f994 |
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| Quellennotiz | uspto-grants-1986_05 |
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