HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30944Generated: October 26, 2026
Epichlorohydrin → n-Glycidyl-n-methylperfluorobutanesulfonamide
https://huagongshe.com/reaction/30944
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | 1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamide | HCID 109968 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Product | n-Glycidyl-n-methylperfluorobutanesulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07425374B2 |
|---|
| Source dataset | uspto-grants-2008_09 |
|---|
| ORD ID | ord-1f5e343d782049eb898ffc2a5fc38393 |
|---|
| Source note | uspto-grants-2008_09 |
|---|