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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513683Generated: October 26, 2026

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

https://huagongshe.com/reaction/1513683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantMethylamineHCID 6329—
Reactant1,1-DichloroethaneHCID 6365—
Reactant5-BromophthalideHCID 603144—
ReactantAluminum(III) ChlorideHCID 6451240—
Product4-bromo-2-(hydroxymethyl)-N-methylbenzamideHCID 5769104859.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 500 mL RB flask was charged with aluminum(III) chloride (4.1 g, 31 mmol) and 10 mL of 1,2-dichloroethane (99 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217177B2
Source datasetuspto-grants-2012_07
ORD IDord-79f8e7459bb7498fb39121b3b2a21fb6
Source noteuspto-grants-2012_07