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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 743936생성일: 2026년 10월 26일

Pyridine → 3a,4,7,7a-tetrahydro-2-(((trifluoromethyl)sulfonyl)oxy)-4,7-methano-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/743936

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dioneHCID 89529—
용매DichloromethaneHCID 6344—
생성물3a,4,7,7a-tetrahydro-2-(((trifluoromethyl)sulfonyl)oxy)-4,7-methano-1H-isoindole-1,3(2H)-dioneHCID 990129098%

반응 단계

To a solution of trifluoromethanesulfonic anhydride (6.5 g, 23 mmole) in methylene chloride (20 ml), a solution of N-hydroxy-bicyclo[2,2,1]-hept-5-ene-2,3-dicarboximide (3.6 g, 20 mmole) and pyridine (1.6 g) in methylene chloride (10 ml) was added dropwise at 0°-5° C. and continued to stir for 15 minutes at the same temperature. The reaction mixture was washed with H2O (20 ml×3), dried over anhydrous Mg SO4 and evaporated. The residue was recrystallized from ethanol to give 6.1 g of N-trifluoromethanesulfonyloxy-bicyclo[2,2,1]-hept-5-ene-2,3-dicarboximide as white needles. m.p. 89°-90° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05558971
출처 데이터셋uspto-grants-1996_09
ORD IDord-5627bca184b24259a99b7bb1017d4548
출처 메모uspto-grants-1996_09