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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512078생성일: 2026년 10월 25일

Methanesulfonamide → 2,4,5-trifluoro-N-(methylsulfonyl)benzamide

https://huagongshe.com/reaction/512078

반응식

참여 물질

역할이름HCID투입량
반응물MethanesulfonamideHCID 72879—
반응물DiisopropylethylamineHCID 81531—
반응물Propylphosphonic anhydrideHCID 111923—
반응물2,4,5-Trifluorobenzoic acidHCID 521170—
반응물N,N-dimethylformamide ethyl acetateHCID 22989253—
용매TetrahydrofuranHCID 8028—
생성물2,4,5-trifluoro-N-(methylsulfonyl)benzamideHCID 5804243572%

반응 단계

2,4,5-Trifluorobenzoic acid (3.00 g, 17.0 mmol), N-ethyl-N-isopropylpropan-2-amine (8.9 mL, 6.6 g, 51.1 mmol), 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxide 50% solution in EtOAc/DMF (12.7 mL, 13.6 g, 42.6 mmol) and methanesulfonamide (3.24 g, 34.1 mmol) were suspended in THF (40 mL) and stirred under a nitrogen atmosphere at reflux for 18 hours. The reaction mixture was cooled, concentrated in vacuo and the residue suspended in water (pH=4). The mixture was acidified to pH=2 with an aqueous solution of potassium hydrogen sulfate (0.5 M). The mixture was extracted with EtOAc (1×100 mL). The organic layer was washed with brine (2×50 mL), dried over sodium sulfate, filtered and evaporated to yield the crude solid. The crude solid was triturated with hexane to yield the title compound as an off-white crystalline solid (3.08 g, 72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102621B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-ae3ee945d1d34237a7f0a936d30ca45a
출처 메모uspto-grants-2015_08