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HRID 219112作成日:2026年10月26日

1,2-Dichloroethane → 4-bromo-2-(hydroxymethyl)-N-methylbenzamide

https://huagongshe.com/reaction/219112

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物MethylamineHCID 6329—
反応物1,1-DichloroethaneHCID 6365—
反応物5-BromophthalideHCID 603144—
反応物Aluminum(III) ChlorideHCID 6451240—
生成物4-bromo-2-(hydroxymethyl)-N-methylbenzamideHCID 5769104859.5%

反応条件

温度0 °C

反応手順

A 500 mL RB flask was charged with aluminum(III) chloride (4.1 g, 31 mmol) and 10 mL of 1,2-dichloroethane (90 ml, 1142 mmol), then cooled to 0° C. A separate 250 mL flask was charged with 90 mL of 1,2-dichloroethane (90 ml, 1142 mmol) and cooled to 0° C.; methylamine (gas) (1.8 g, 59 mmol) was bubbled through the solution for 10 minutes. The dichloroethane solution was slowly poured into the aluminum chloride solution, resulting in the formation of a thick white slush. This was warmed to room temperature. 5-bromoisobenzofuran-1(3H)-one (5.00 g, 23 mmol) was added in one portion and the reaction mixture was stirred for 2.5 hours and quenched with water. The mixture was filtered to remove the solid impurities, then the filtrate was washed with 0.5N aqueous HCl (100 mL) and brine (200 mL). The organic layer was dried with MgSO4, filtered, and concentrated to give a white solid. This was triturated with EtOAc and filtered to give 4-bromo-2-(hydroxymethyl)-N-methylbenzamide (3.34 g, 58% yield) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198448B2
出典データセットuspto-grants-2012_06
ORD IDord-2ac03fe6c82240fc95b6ff0a4d7e54a4
出典メモuspto-grants-2012_06