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HRID 29660作成日:2026年10月24日

Triethylamine → 2-(4-Tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl ester

https://huagongshe.com/ja/reaction/29660

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-tert-Butylbenzoyl chlorideHCID 74372—
反応物Methyl 4-nitroanthranilateHCID 596476—
溶媒DichloromethaneHCID 6344—
溶媒Sodium chloride; waterHCID 57417360—
生成物2-(4-Tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl esterHCID 6919452960%

反応手順

To a solution of 4-nitro-anthranilic acid methyl ester (1.500 g, 7.4 mmol) in CH2Cl2 (200 mL) was added triethylamine (8 mL) and 4-tert-butyl benzoyl chloride and the reaction was stirred overnight at rt. It was then poured into brine, extracted with ethyl acetate, dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography using ethyl acetate/hexanes (20/80) to afford 2-(4-tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl ester (1.841 g, 60%) as a yellow solid. mp=146.0-148.4° C.; mass spectrum (−ES, M−H) in/z 355. 1H NMR (400 MHz, DMSO-d6); δ 11.60 (bs, 1H), 9.35 (d, 1H), 8.20 (d, 1H), 8.02 (dd, 1H), 7.90 (d, 2H), 7.64 (d, 2H), 3.95 (s, 3H), 1.36 (s, 9H). Elemental analysis: Calcd. for C19H20N2O5: C, 64.04; H, 5.66; N, 7.86, Found: C, 64.04; H, 5.79; N, 7.76.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420083B2
出典データセットuspto-grants-2008_09
ORD IDord-72ec1c9158684e528be265558f7462da
出典メモuspto-grants-2008_09