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HRID 52297作成日:2026年10月24日

Dichloromethane → 4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamide

https://huagongshe.com/ja/reaction/52297

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物4-FluoroanilineHCID 9731—
反応物4-(Methylsulfonyl)benzonitrileHCID 519981—
反応物TrimethylaluminumHCID 16682925—
溶媒TolueneHCID 1140—
溶媒ChloroformHCID 6212—
生成物4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamideHCID 17850476335%

反応手順

To a suspension of 4-fluoroaniline (4 mL, 40 mmol) in toluene (120 mL), trimethylaluminum (2M solution in toluene, 21 mL, 42 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 3 hours. A solution of 4-(methylsulfonyl)benzonitrile (7.65 g, 40 mmol) in methylene chloride (100 mL) was added over 10 minutes and the reaction mixture was heated to 70°-75° C. After 48 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 crude intermediate (7.7 g) was chromatographed [silica gel, hexane/ethyl acetate, 25/75] to give 4-methylsulfonyl-N-[4-chlorophenyl]benzenecarboximidamide (4.1 g, 35%) as a white solid: mp (DSC) 182° C. Anal. Calc'd. for C14H13N2SO2F: C, 57.52, H, 4.48, N, 9.58, S, 10.97. Found: C, 57.37, H, 4.69, N, 9.21, S, 10.69.

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-79d9344789514a02b4037e46ddef742f
出典メモuspto-grants-1997_04