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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1352944생성일: 2026년 10월 25일

p-Toluenesulfonic acid monohydrate → 2-Benzo[1,3]dioxol-5-yl-1-(4-methanesulfonyl-phenyl)-4-trifluoromethyl-1H-imidazole

https://huagongshe.com/reaction/1352944

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물5-[1-[4-(methylsulfonyl)phenyl]-4-hydroxy-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl)-1,3-benzodioxoleHCID 10598616—
용매TolueneHCID 1140—
생성물2-Benzo[1,3]dioxol-5-yl-1-(4-methanesulfonyl-phenyl)-4-trifluoromethyl-1H-imidazoleHCID 1078769880%

반응 단계

A mixture of 5-[1-[4-(methylsulfonyl)phenyl]-4-hydroxy-4-(trifluoromethyl)-4,5-dihydro-1H-imidazol-2-yl]-1,3-benzodioxole from Step 2 (1.26 g, 2.9 mmol) and p-toluenesulfonic acid monohydrate (200 mg) in toluene (50 mL) was heated to reflux for 72 hours. The reaction mixture was cooled and the solvent removed under reduced pressure. The crude residue was redissolved in methylene chloride and washed with water, aqueous sodium bicarbonate and brine. After drying (Na2SO4), filtration and concentration in vacuo, the crude mixture (1.34 g) was purified by chromatography on silica gel using toluene/ethyl acetate 1/1 to give pure 5-(1-(4-(methylsulfonyl)phenyl)-4-(trifluoromethyl)-1H-imidazol-2-yl]-1,3-benzodioxole (940 mg, 80%) as a white solid: mp (DSC) 165° C. Anal Calc'd. for C18H13N2SO4F3: C, 52.68; H, 3.19; No 6.83. Found: C, 53.05; H, 3.19; N, 6.65.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07220770B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-b95842a6bb264da6b999789e4e395504
출처 메모uspto-grants-2007_05