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HRID 382347作成日:2026年10月27日

Ammonia → 2-Carbamoyl-3-nitrobenzoic acid

https://huagongshe.com/reaction/382347

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物3-Nitrophthalic anhydrideHCID 21631—
反応物Ammonium 2-(aminocarbonyl)benzoateHCID 3083555—
生成物2-Carbamoyl-3-nitrobenzoic acidHCID 437547—

反応条件

温度30 °C

反応手順

3-Nitrophthalic anhydride (10.0 g, 50 mmol) was added in portions over 20 minutes to concentrated aqueous ammonia solution (15 ml), and the mixture was stirred at 30° C. for a further 30 minutes. The crystalline mass of ammonium phthalamate, deposited upon cooling the pale yellow solution, was collected and redissolved in a minimum amount of warm water. Concentrated hydrochloric acid (4.5 ml) was added dropwise, with stirring, and the resulting paste was washed with water, and dried in vacua to give 3-nitrophthalamic acid as a fine white powder. (9.01 g, 83%), m.p. 217° C. Found: C, 45.76; H, 2.79; N, 13.21. C8H6N2O5 requires C, 45.71; H, 2.86; N, 13.33%; vmax/cm−1 3466.52, 3321.84, 1668.64, 1604.98, and 1525.89; δH (d6-DMSO, 200 MHz) 7.75 (1H, br s, CONH), 7.8 (1H, t, Ar-5H), 8.16 (1H, brs, CONH), 8.2 (1H, d, Ar-6H), 8.3 (1H, d, Ar-4H); δC (d6-DMSO) 127.32, 130.06, 132.28, 133.49, 134.78, 147.71, 166.25, and 166.60; m/z (EI) 192 (M+−1), 177, 149, 103, 75.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06310082B1
出典データセットuspto-grants-2001_10
ORD IDord-a9b598bfa42e4ccda7cc03d0593a5c0e
出典メモuspto-grants-2001_10