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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1352958생성일: 2026년 10월 26일

p-Tolunitrile → HCID 178425632, 화합물

https://huagongshe.com/reaction/1352958

반응식

참여 물질

역할이름HCID투입량
반응물p-TolunitrileHCID 7724—
반응물4-(Methylsulfonyl)anilineHCID 79617—
반응물TrimethylaluminumHCID 16682925—
용매TolueneHCID 1140—
용매ChloroformHCID 6212—
생성물HCID 178425632HCID 178425632—

반응 단계

To a suspension of 4-(methylsulfonyl)aniline (3.57 g, 20.9 mmol) in toluene (150 mL), trimethylaluminum (15.6 ml, 2M solution in toluene, 31.4 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 4-methylbenzonitrile (5 ml, 41.8 mmol) in toluene (100 mL) was added over 10 minutes and the reaction mixture 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 residue was washed with a mixture of methylene chloride/methanol (2/1). The combined filtrates are concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 600 mL). The intermediate was filtered and washed with more of hexane/ether (2/1). The pale yellow solid 4-methyl-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (5.3 g, 88%) was used in the next reaction without further purification: mp (DSC) 213° C. Anal. Calc'd for C15H16N2SO2: C, 62.48; H, 5.59; N, 9.71. Found: C, 62.00; H, 5.52; N, 9.60.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07220770B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-ef0ecb3acd724240b68531bbd4653496
출처 메모uspto-grants-2007_05