戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7735作成日:2026年10月24日

2-Aminophenol → 3,5-dimethoxy-N-(2-methoxyphenyl)-4-methylbenzamide

https://huagongshe.com/ja/reaction/7735

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminophenolHCID 5801—
反応物Thionyl ChlorideHCID 24386—
反応物DiisopropylethylamineHCID 81531—
反応物3,5-Dimethoxy-4-methylbenzoic acidHCID 3764486—
溶媒TetrahydrofuranHCID 8028—
生成物3,5-dimethoxy-N-(2-methoxyphenyl)-4-methylbenzamideHCID 2599339—

反応手順

Thionyl chloride (10 mL) and 3,5-dimethoxy-4-methylbenzoic acid (1.0 g, 5.1 mmol) was refluxed under argon until no starting material was observed by TLC. After cooling reaction mixture to rt, concentrated mixture in vacuo. The resulting brown oil was added to a mixture of 2-aminophenol (580 mg, 5.3 mmol), diisopropylethyl amine (1.1 mL, 6.3 mmol) and THF (40 mL) at 0° C. and then brought to rt overnight. After concentrating mixture in vacuo, the resulting brown oil was purified by flash chromatography on silica gel, using a gradient elution from 1:9 EtOAc:hexanes to 1:1 EtOAc:hexanes. This afforded the desired intermediate, 3,5-dimethoxy-N-(2-methoxyphenyl)-4-methylbenzamide, as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087601B2
出典データセットuspto-grants-2006_08
ORD IDord-6aab020e505c4013a9621c93cb7e9ea8
出典メモuspto-grants-2006_08