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HRID 30944作成日:2026年10月24日

Epichlorohydrin → n-Glycidyl-n-methylperfluorobutanesulfonamide

https://huagongshe.com/ja/reaction/30944

反応式

関与物質

役割名称HCID仕込み量
反応物EpichlorohydrinHCID 7835—
反応物1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamideHCID 109968—
反応物HCID 178418582HCID 178418582—
生成物n-Glycidyl-n-methylperfluorobutanesulfonamideHCID 86614459—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425374B2
出典データセットuspto-grants-2008_09
ORD IDord-1f5e343d782049eb898ffc2a5fc38393
出典メモuspto-grants-2008_09