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HRID 18896作成日:2026年10月24日

Hydrochloric Acid → N-(2-benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamide

https://huagongshe.com/ja/reaction/18896

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物p-Bromobenzenesulfonyl chlorideHCID 7396—
反応物2-Amino-5-chlorobenzophenoneHCID 12870—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒Ethyl AcetateHCID 8857—
生成物N-(2-benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamideHCID 333475798.4%

反応手順

2-Amino-5-chlorobenzophenone (5.33 g, 23 mmol) was dissolved in 100 mL pyridine and stirred at room temperature. 4-Bromobenzenesulfonyl chloride (6.17 g, 24.1 mmol) was added and the mixture was stirred overnight. The mixture was poured in a steady stream into 350 mL vigorously stirring chilled 6M HCl which resulted in the precipitation of a reddish oil. The solution was diluted with 100 mL EtOAc and 200 mL H2O, shaken in a separating funnel and the aqueous layer discarded. The organics were dried and reduced in vacuo to yield title compound (10.2 g, 98%). 1H NMR (400 MHz, CDCl3): δ 7.34 (m, 5H), 7.43-7.48 (m, 5H), 7.62 (t, 1H), 7.74 (d, 1H), 9.62 (s, 1H). MS: m/z=449.9 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741519B2
出典データセットuspto-grants-2010_06
ORD IDord-26c50f35ca01425f953f3b1789ffe2e9
出典メモuspto-grants-2010_06