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HRID 55301作成日:2026年10月26日

Benzenesulfonamide → 4-Iodo-N-(phenylsulfonyl)benzamide

https://huagongshe.com/reaction/55301

反応式

関与物質

役割名称HCID仕込み量
反応物BenzenesulfonamideHCID 7370—
反応物4-Iodobenzoic acidHCID 12085—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物4-Iodo-N-(phenylsulfonyl)benzamideHCID 448683140.4%

反応手順

5 g of 4-iodobenzoic acid is added to a solution of 3.3 g of benzenesulfonamide, 2.68 g of 4-dimethylaminopyridine and 4.04 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide in 100 ml of dichloromethane, and the suspension is stirred for 18 hours at room temperature. The reaction mixture is diluted with 400 ml of dichloromethane, washed in succession with 400 ml portions of 10% hydrochloric acid, water and saturated common salt solution, the organic phase is dried on sodium sulfate and concentrated by evaporation. The residue is suspended in diethyl ether/ethyl acetate=1/1, and the crystallizate is suctioned off. 3.15 g of N-benzenesulfonyl-4-iodobenzoic acid amide of melting point 192°-193° C. is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624943
出典データセットuspto-grants-1997_04
ORD IDord-b52ab99c986e4c808f849a844c91cd95
出典メモuspto-grants-1997_04