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HRID 52312作成日:2026年10月26日

4-(Methylsulfonyl)aniline → HCID 178425633、化合物

https://huagongshe.com/reaction/52312

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Methylsulfonyl)anilineHCID 79617—
反応物3-Chloro-p-toluonitrileHCID 88894—
反応物TrimethylaluminumHCID 16682925—
溶媒TolueneHCID 1140—
溶媒ChloroformHCID 6212—
生成物HCID 178425633HCID 178425633—

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 3-chloro-4-methylbenzonitrile (5 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, 700 mL). The intermediate was filtered and washed with more of hexane/ether (2/1). The pale yellow solid 3-chloro-4-methyl-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (4.7 g, 88%) was used in the next reaction without further purification: mp (DSC) 179° C. Anal. Calc'd. for C15H15N2SO2Cl: C, 55.81, H, 4.68, N, 8.68. Found: C, 55.65, H, 4.63, N, 8.59.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616601
出典データセットuspto-grants-1997_04
ORD IDord-b3b0a34bbebd4c4f8d05de58db324efd
出典メモuspto-grants-1997_04