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HRID 7681作成日:2026年10月26日

2-Aminophenol → 3-bromo-N-(2-hydroxyphenyl)4-methylbenzamide

https://huagongshe.com/reaction/7681

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-Bromo-4-methylbenzoic acidHCID 82130—
溶媒TetrahydrofuranHCID 8028—
生成物3-bromo-N-(2-hydroxyphenyl)4-methylbenzamideHCID 21990965—

反応手順

A mixture of 3-bromo-4-methylbenzoic acid (1.0 g, 4.7 mmol) and thionyl chloride (18 mL) was refluxed for 1 h and then cooled to rt. The excess thionyl chloride was removed in vacuo, the residue was dissolved in THF (10 mL), and was added to a cooled (0° C.) mixture of 2-aminophenol (510 mg, 4.7 mmol) and diisopropylethylamine (0.90 mL, 5.1 mmol) in THF (18 mL). The resulting mixture was stirred at rt for 4 h. The solvent was then removed and the residue was purified by flash chromatography on silica gel eluting with EtOAc:hexane (1:5 to 1:4) to afford 3-bromo-N-(2-hydroxyphenyl)-4-methylbenzamide.

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-e4a2a72cc2724411b370e0075895332a
出典メモuspto-grants-2006_08