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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52304생성일: 2026년 10월 24일

p-Chlorophenacyl bromide → 2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole

https://huagongshe.com/ko/reaction/52304

반응식

참여 물질

역할이름HCID투입량
반응물p-Chlorophenacyl bromideHCID 68303—
반응물Sodium BicarbonateHCID 516892—
반응물4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—
용매IsopropanolHCID 3776—
생성물2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazoleHCID 2214896955%

반응 단계

To a mixture of 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, Step 1) (700 mg, 2.24 mmol) and sodium bicarbonate (376 mg, 4.48 mmol) in isopropanol (30 mL), 4-chlorophenacyl bromide (1.05 g, 4.48 mmol) was added. After heating the reaction mixture at 80°-85° C. for 18 hours, the solvent was removed. The residue was redissolved in methylene chloride and washed with aqueous sodium bicarbonate and water. The organic fractions were combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was chromatographed (silica gel, hexane/ethyl acetate, 6/4) to give 2,4-bis-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-1H-imidazole (545 mg, 55%) as a pale yellow solid: mp 169°-171° C. Anal. Calc'd. for C22H16N2SO2Cl12 : C, 59.60, H, 3.64, N, 6.32, S, 7.23. Found: C, 59.86, H, 3.80, N, 6.10, S, 7.27.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616601
출처 데이터셋uspto-grants-1997_04
ORD IDord-ac86626c127242c192cab62d8b87aacd
출처 메모uspto-grants-1997_04