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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41393생성일: 2026년 10월 23일

P-Toluenesulfonamide → 4,7-Difluoro-2-(toluene-4-sulfonyl)isoindoline

https://huagongshe.com/ko/reaction/41393

반응식

참여 물질

역할이름HCID투입량
반응물P-ToluenesulfonamideHCID 6269—
반응물Sodium hydrideHCID 24758—
반응물2,3-Bis-bromomethyl-1,4-difluorobenzeneHCID 59382290—
용매DimethylformamideHCID 6228—
생성물4,7-Difluoro-2-(toluene-4-sulfonyl)isoindolineHCID 5938224856%

반응 조건

온도110 °C

반응 단계

A solution of 4-toluenesulphonamide (2.44 g, 14.28 mmol) in N,N-dimethylformamide (10 ml) was added dropwise to a vigourously stirred suspension of sodium hydride (1.2 g, 60 wt % in mineral oil, 30.0 mmol) in anhydrous N,N-dimethylformamide (60 ml). The mixture was stirred at room temperature for 1 hour, at 110° C. for 1 hour and was then cooled to 60° C. and a solution of 2,3-bis-bromomethyl-1,4-difluorobenzene (4.28 g, 14.28 mmol) in N,N-dimethylformamide (30 ml) was added dropwise. The mixture was stirred at 60° C. for 1 hour and then at room temperature for 16 hours. The solvent was removed in vacuo and the residue partitioned between dichloromethane and 1M hydrochloric acid. The organic layer was separated, washed with 5% aqueous potassium carbonate solution, the organics were separated and the solvent removed in vacuo. The residue was rinsed with diethyl ether, filtered and the solids sucked dry under reduced pressure to afford 4,7-difluoro-2-(toluene-4-sulfonyl)isoindoline (2.46 g, 56%) as a pale tan solid. 1H NMR (DMSO-d6) 7.82 (2H, d), 7.43 (2H, d), 7.15 (2H, dd), 4.66 (4H, s), 2.36 (3H, s). MS: [M+H]+ 310.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530469B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-28f6d75c693543f6ad7c911c7f8a0896
출처 메모uspto-grants-2013_09