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HRID 52294作成日:2026年10月23日

4-Chlorobenzonitrile → 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide

https://huagongshe.com/ja/reaction/52294

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorobenzonitrileHCID 12163—
反応物4-(Methylsulfonyl)anilineHCID 79617—
反応物TrimethylaluminumHCID 16682925—
溶媒TolueneHCID 1140—
溶媒ChloroformHCID 6212—
生成物4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—

反応手順

To a suspension of 4-(methylsulfonyl)aniline (7 g, 41 mmol) in toluene (400 mL), trimethylaluminum (2M solution in toluene, 30.5 mL, 61 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 4-chlorobenzonitrile (11.3 g, 82 mmol) in toluene (200 mL) was added over 10 minutes and the reaction mixture was heated to 80°-85° C. After 16 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. 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 intermediate was filtered and washed with more of hexane/ether (2/1). The pale yellow solid 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (10.93 g, 86%) was used in the next reaction without further purification: mp (DSC) 191° C. Anal. Calc'd. for C14H13N2SO2Cl: C, 54.46, H, 4.24, N, 9.07. Found: C, 54.42, H, 4.30, N, 9.07.

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-45e2e30cff9d4228995f8b63eba08d26
出典メモuspto-grants-1997_04