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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530216Generated: November 4, 2026

Methyl iodide → Methyl 5-bromo-3-(cyclohexyl(methyl)amino)-2-methylbenzoate

https://huagongshe.com/reaction/1530216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 5-bromo-3-(cyclohexylamino)-2-methylbenzoateHCID 70872336—
SolventAcetonitrileHCID 6342—
ProductMethyl 5-bromo-3-(cyclohexyl(methyl)amino)-2-methylbenzoateHCID 7087243787%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of methyl 5-bromo-3-(cyclohexylamino)-2-methylbenzoate (2.75 g, 8.45 mmol) in acetonitrile (25 mL), cesium carbonate (5.45 g, 16.9 mmol) and methyl iodide (6 g, 42.3 mmol) were added; resulting solution was heated at 80° C. for 20 h. On completion, the solution was cooled to room temperature and filtered, and the residue was washed with ethyl acetate. The filtrate was concentrated and then purified by column chromatography to afford methyl 5-bromo-3-(cyclohexyl(methyl)amino)-2-methylbenzoate (2.5 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090562B2
Source datasetuspto-grants-2015_07
ORD IDord-de8e67738bbc4c67b06d4eac27d3489f
Source noteuspto-grants-2015_07