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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1352942생성일: 2026년 10월 27일

Benzo-1,3-dioxole-5-carbonitrile → HCID 178504792, 화합물

https://huagongshe.com/reaction/1352942

반응식

참여 물질

역할이름HCID투입량
반응물Benzo-1,3-dioxole-5-carbonitrileHCID 78136—
반응물4-(Methylsulfonyl)anilineHCID 79617—
반응물TrimethylaluminumHCID 16682925—
용매TolueneHCID 1140—
용매ChloroformHCID 6212—
생성물HCID 178504792HCID 178504792—

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 piperonylonitrile (4.85 g, 33 mmol) in toluene (100 mL) was added over 10 minutes and the reaction mixture was heated to 90–95° 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 were concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 1000 mL). The product was filtered and washed with more of hexane/ether (2/1). The pale yellow solid 3,4-methylenedioxy-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (4.8 g, 91%) was used in the next reaction without further purification: mp (DSC) 214° C. Anal. Calc'd. for C15H14N2SO4: C, 56.59; H, 4.43; N, 8.80. Found: C, 56.33; H, 4.28; N, 8.66.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07220770B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-88771ad6cf6d4d70b18a6d67a72a4412
출처 메모uspto-grants-2007_05