戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 74157作成日:2026年10月23日

Hydrochloric Acid → 4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acid

https://huagongshe.com/ja/reaction/74157

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TriethylamineHCID 8471—
反応物4-Fluoro-3-nitrobenzoic acidHCID 67987—
反応物4-AminotetrahydropyranHCID 419223—
反応物Oxan-2-amineHCID 14471248—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acidHCID 43610332101.2%

反応手順

4-Fluoro-3-nitrobenzoic acid (126.4 g, 0.68 mol) was dissolved in ethanol (880 mL). Triethylamine (82.6 g, 0.82 mol), 4-aminotetrahydropyran (82.7 g, 0.81 mol) were added in turn dropwise, and after the additions the reaction solution was heated to reflux. After refluxing for 5 h, triethylamine (8.3 g, 82 mmol), aminotetrahydropyran (8.3 g, 81 mmol) were added, and this was refluxed for a further 9 hours. After the reaction mixture was allowed to cool to room temperature, 2N HCl (880 mL) and water (880 mL) were added and after stirring for awhile, the solid obtained was filtered off. This was forced air-dried at 60° C. to yield the title compound (183.3 g, quant.) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829035B2
出典データセットuspto-grants-2014_09
ORD IDord-3d585bfc7faf417584411f9094ad5215
出典メモuspto-grants-2014_09