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HRID 219112생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/219112

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물MethylamineHCID 6329—
반응물1,1-DichloroethaneHCID 6365—
반응물5-BromophthalideHCID 603144—
반응물Aluminum(III) ChlorideHCID 6451240—
생성물4-bromo-2-(hydroxymethyl)-N-methylbenzamideHCID 5769104859.5%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198448B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-2ac03fe6c82240fc95b6ff0a4d7e54a4
출처 메모uspto-grants-2012_06