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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811002Generated: November 1, 2026

3-Bromo-o-toluidine → Methyl 2-((3-bromo-2-methylphenylamino)methyl)-5-methoxybenzoate

https://huagongshe.com/reaction/1811002

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-o-toluidineHCID 123538—
ReactantMethyl 2-(bromomethyl)-5-methoxybenzoateHCID 53407594—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-((3-bromo-2-methylphenylamino)methyl)-5-methoxybenzoateHCID 6660618918%

Reaction Conditions

Temperature85 °C

Reaction Steps

Step 2 A mixture of methyl 2-(bromomethyl)-5-methoxybenzoate (1.435 g, 5.54 mmol), 3-bromo-2-methylaniline (1.03 g, 5.54 mmol) and TEA (1.158 mL, 8.31 mmol) in methanol (5 mL) was heated at 85° C. for 2 h. The mixture was diluted with DCM, washed with NaHCO3 (aq), and dried and concentrated. The residue was purified by column chromatography (eluting with EtOAc-hexane) to provide methyl 2-((3-bromo-2-methylphenylamino)methyl)-5-methoxybenzoate as a yellow oil (361 mg, 18%). Mass spectrum m/z 364, 366 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-787ab899325348659409abe5da934008
Source noteuspto-grants-2013_01