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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661822Generated: November 1, 2026

3-Bromo-o-toluidine → HCID 66605859, compound

https://huagongshe.com/reaction/661822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-o-toluidineHCID 123538—
Reactant3-Oxo-1,3-dihydro-2-benzofuran-5-carbonitrileHCID 13289562—
ReactantTrimethylaluminumHCID 16682925—
SolventDichloromethaneHCID 6344—
ProductHCID 66605859HCID 6660585914%

Reaction Steps

Step 1 A solution of 3-bromo-2-methylaniline (0.67 g, 3.60 mmol) in DCM (18 mL) was treated dropwise with trimethylaluminum (2 M in toluene, 1.801 mL, 3.60 mmol) and the resulting solution was stirred at rt for 30 min. A solution of 3-oxo-1,3-dihydroisobenzofuran-5-carbonitrile (0.573 g, 3.60 mmol) in DCM (18.00 mL) was added and the resulting mixture was stirred at rt overnight. The mixture was diluted with DCM, washed with an aqueous solution of sodium potassium tartrate (Fehling's Reagent II) and water, then was dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 80:20 hexane-EtOAc to EtOAc) to provide N-(3-bromo-2-methylphenyl)-5-cyano-2-(hydroxymethyl)benzamide as a white solid (170 mg, 14%) which was used without further purification. Mass spectrum m/z 345, 347 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084620B2
Source datasetuspto-grants-2011_12
ORD IDord-de5b68f09dab4ed583c98ee5615747e4
Source noteuspto-grants-2011_12