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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30944Generated: October 26, 2026

Epichlorohydrin → n-Glycidyl-n-methylperfluorobutanesulfonamide

https://huagongshe.com/reaction/30944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
Reactant1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamideHCID 109968—
ReactantHCID 178418582HCID 178418582—
Productn-Glycidyl-n-methylperfluorobutanesulfonamideHCID 86614459—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425374B2
Source datasetuspto-grants-2008_09
ORD IDord-1f5e343d782049eb898ffc2a5fc38393
Source noteuspto-grants-2008_09