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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52316생성일: 2026년 10월 24일

4-(Methylsulfonyl)aniline → HCID 178491240, 화합물

https://huagongshe.com/ko/reaction/52316

반응식

참여 물질

역할이름HCID투입량
반응물4-(Methylsulfonyl)anilineHCID 79617—
반응물3-Fluoro-4-methoxybenzonitrileHCID 2774548—
반응물TrimethylaluminumHCID 16682925—
용매TolueneHCID 1140—
용매ChloroformHCID 6212—
생성물HCID 178491240HCID 178491240—

반응 단계

To a suspension of 4-(methylsulfonyl)aniline (2.82 g, 16.5 mmol) in toluene (150 mL), trimethylaluminum (2M solution in toluene, 12.5 mL, 24.7 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 3-fluoro-4-methoxybenzonitrile (5 g, 33 mmol) in toluene (100 mL) was added over 10 minutes and the reaction mixture was heated to 80°-85° C. After 20 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the reside was washed with a mixture of methylene chloride/methanol (2/1). The combined filtrates were concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 1000 mL). The intermediate was filtered and washed with more hexane/ether (2/1). The pale yellow solid 3-fluoro-4-methoxy-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (3.95 g, 74%) was used in the next reaction without further purification: mp (DSC) 195° C. Anal. Calc'd. for C15H15N2SO3F: C, 55.89, H, 4.69, N, 8.69. Found: C, 55.92, H, 4.74, N, 8.53.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616601
출처 데이터셋uspto-grants-1997_04
ORD IDord-4f3accbe569b48688531b22fb862f88a
출처 메모uspto-grants-1997_04