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HRID 1603613作成日:2026年10月24日

Acetic Anhydride → N-(3-bromo-5-nitrophenyl)acetamide

https://huagongshe.com/ja/reaction/1603613

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物ar-Bromo-ar-nitrobenzenamineHCID 44535—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物N-(3-bromo-5-nitrophenyl)acetamideHCID 1065890891.5%

反応手順

28.40 g (0.131 mol) of 3-bromo-5-nitroaniline were dissolved in 250 ml of pyridine and treated with 30 ml (0.317 mol) of acetic anhydride. The mixture was stirred at room temperature for 18 hrs. and subsequently at 40° C. for 2 hrs. Then, the residue was digested in water and the precipitate was filtered off. The filter material was rinsed with a large amount of water and dried at 45° C. in a high vacuum. There were obtained 31.0 g (91.5%) of N-(3-bromo-5-nitrophenyl)-acetamide as orange-yellow crystals. MS (ISP): me/e=260, 258 (C8H8BrN2O3+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05990105
出典データセットuspto-grants-1999_11
ORD IDord-849c30a95b584c4cb3098744679e5144
出典メモuspto-grants-1999_11