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HRID 1166331作成日:2026年10月24日

Benzo-1,3-dioxole-5-carbonitrile → HCID 178504792、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物Benzo-1,3-dioxole-5-carbonitrileHCID 78136—
反応物4-(Methylsulfonyl)anilineHCID 79617—
反応物TrimethylaluminumHCID 16682925—
溶媒TolueneHCID 1140—
溶媒ChloroformHCID 6212—
生成物HCID 178504792HCID 178504792—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06613789B2
出典データセットuspto-grants-2003_09
ORD IDord-31131d431e984723bc57a8799154a5a5
出典メモuspto-grants-2003_09