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HRID 14458作成日:2026年10月25日

Triethylamine → HCID 68703339、化合物

https://huagongshe.com/reaction/14458

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Isobutyryl chlorideHCID 62325—
反応物2-(4-Chlorophenyl)-1-(3,4-difluoro-2-hydroxy-phenyl)-ethanoneHCID 68698513—
溶媒DichloromethaneHCID 6344—
生成物HCID 68703339HCID 68703339—

反応手順

A solution of 2-(4-chlorophenyl)-1-(3,4-difluoro-2-hydroxy-phenyl)-ethanone (4.5 g, 87% pure, 13.85 mmol) and triethylamine (1.7 g, 2.35 ml, 16.8 mmol, 1.2 eq.) in methylene chloride (100 ml) is treated dropwise at ambient temperature with isobutyryl chloride (1.79 g, 1.76 ml, 16.8 mmol, 1.2 eq.). After stirring for 5 h, the solution is washed successively with 2M HCl solution and saturated sodium hydrogen carbonate solution. The organic phase is dried over anhydrous magnesium sulphate, filtered and evaporated to dryness in vacuo to afford a black residue. This is triturated with methanol at room temperature overnight to afford a brown solid, which is filtered and washed with methanol. The solid is purified twice by flash chromatography (ethyl acetate/cyclohexane=1:9) to furnish the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732435B2
出典データセットuspto-grants-2010_06
ORD IDord-1a5857e3db8c41c8b57535852103d956
出典メモuspto-grants-2010_06