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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30944생성일: 2026년 10월 24일

Epichlorohydrin → n-Glycidyl-n-methylperfluorobutanesulfonamide

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

반응식

참여 물질

역할이름HCID투입량
반응물EpichlorohydrinHCID 7835—
반응물1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamideHCID 109968—
반응물HCID 178418582HCID 178418582—
생성물n-Glycidyl-n-methylperfluorobutanesulfonamideHCID 86614459—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425374B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-1f5e343d782049eb898ffc2a5fc38393
출처 메모uspto-grants-2008_09