HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30944Erstellt: 23. Oktober 2026
Epichlorohydrin → n-Glycidyl-n-methylperfluorobutanesulfonamide
https://huagongshe.com/de/reaction/30944
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Epichlorohydrin | HCID 7835 | — |
| Edukt | 1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamide | HCID 109968 | — |
| Edukt | HCID 178418582 | HCID 178418582 | — |
| Produkt | n-Glycidyl-n-methylperfluorobutanesulfonamide | HCID 86614459 | — |
Reaktionsschritte
N-Methylperfluorobutanesulfonamide (MeFBSA, 313 g, 1.0 mol; preparation described in U.S. Pat. No. 6,664,354, Savu et al., Example 1, Part A) was added to a stirred mixture of 220 g NaOCH3 (1.02 mol; 25% NaOMe in MeOH). The solvent was removed under vacuum (pot temperature about 80° C.; 50 mm Hg). The resulting paste was dissolved in 250 mL THF and treated with 473 g (5.11 mol) epichlorohydrin and stirred at reflux for 4 hr. GLC analysis showed complete conversion of MeFBSA. The slurry was cooled, washed with water (300 mL) and the resulting lower layer was taken up in methylene chloride, rewashed with water (300 mL), and dried over MgSO4. The product was stripped and one-plate distilled to a main cut of MeFBSG as a colorless liquid (260.8 g, bp 95-105° C./0.3 mmHg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07425374B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-1f5e343d782049eb898ffc2a5fc38393 |
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| Quellennotiz | uspto-grants-2008_09 |
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