돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535211생성일: 2026년 10월 24일

Sodium Carbonate → C4F9SO2-N(CH3)CH2CH2-NH2

https://huagongshe.com/ko/reaction/535211

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Ethyl-2-oxazolineHCID 66412—
반응물1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamideHCID 109968—
생성물C4F9SO2-N(CH3)CH2CH2-NH2HCID 86649493—
생성물N-(2-(N-methylnonafluorobutanesulfonamido)ethyl)propionamideHCID 86657621—

반응 조건

온도140 °C

반응 단계

C4F9SO2—N(CH3)CH2CH2—NH2 was prepared by the following procedure: N-Methylnonafluorobutanesulfonamide (626 g, 2 moles, 3M Company, St. Paul, Minn.), 2-ethyl-2-oxazoline (198 g, 2 moles, Alfa Aesar, Ward Hill, Mass.), and sodium carbonate (17 g, 0.16 mole, EMD Chemicals, Gibbstown, N.J.) were combined and heated for 16 hours at 140° C. to form N-(2-(N-methylnonafluorobutanesulfonamido)ethyl)propionamide. This amide was twice extracted with 250 mL deionized water, heated for 18 hours at 100° C. with a mixture of 250 mL concentrated hydrochloric acid and 100 mL deionized water, extracted with 925 mL of 24 weight percent aqueous sodium hydroxide solution, extracted with 250 mL 10 weight percent aqueous sodium hydroxide solution, and distilled to provide N-(2-aminoethyl)-N-methylnonafluorobutanesulfonamide (538 g; 75 percent recovery; 94 percent pure by gas chromatography (GC); distilled at 104-109° C. under 2 mm Hg pressure).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08858813B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-d1cfb31d96d4480491bfcdaa5a57b11b
출처 메모uspto-grants-2014_10