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HRID 52294생성일: 2026년 10월 24일

4-Chlorobenzonitrile → 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide

https://huagongshe.com/ko/reaction/52294

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorobenzonitrileHCID 12163—
반응물4-(Methylsulfonyl)anilineHCID 79617—
반응물TrimethylaluminumHCID 16682925—
용매TolueneHCID 1140—
용매ChloroformHCID 6212—
생성물4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—

반응 단계

To a suspension of 4-(methylsulfonyl)aniline (7 g, 41 mmol) in toluene (400 mL), trimethylaluminum (2M solution in toluene, 30.5 mL, 61 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 4-chlorobenzonitrile (11.3 g, 82 mmol) in toluene (200 mL) was added over 10 minutes and the reaction mixture was heated to 80°-85° C. After 16 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol. 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 of hexane/ether (2/1). The pale yellow solid 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (10.93 g, 86%) was used in the next reaction without further purification: mp (DSC) 191° C. Anal. Calc'd. for C14H13N2SO2Cl: C, 54.46, H, 4.24, N, 9.07. Found: C, 54.42, H, 4.30, N, 9.07.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616601
출처 데이터셋uspto-grants-1997_04
ORD IDord-45e2e30cff9d4228995f8b63eba08d26
출처 메모uspto-grants-1997_04