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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1166331생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1166331

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 번호US06613789B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-31131d431e984723bc57a8799154a5a5
출처 메모uspto-grants-2003_09