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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628591Generated: October 31, 2026

Methyl iodide → Methyl 4-chloro-2-[(3-chloropropyl)amino]-3-nitrobenzoate

https://huagongshe.com/reaction/1628591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-2-[(3-chloropropyl)amino]-3-nitrobenzoic acidHCID 68736172—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-chloro-2-[(3-chloropropyl)amino]-3-nitrobenzoateHCID 6873737990%

Reaction Steps

A mixture of 4-chloro-2-[(3-chloropropyl)amino]-3-nitrobenzoic acid (150 mg, 0.512 mmol), methyl iodide (0.0319 mL, 0.512 mmol) and potassium carbonate (70.8 mg, 0.512 mmol) in N,N-dimethylformamide (1.5 mL) was stirred at room temperature for 12 h. After addition of ethyl acetate, the resultant mixture was washed with water and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on NH silica gel eluting with a 5% ethyl acetate/n-hexane mixture to afford a yellow oil (141 mg, 0.459 mmol, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785460B2
Source datasetuspto-grants-2014_07
ORD IDord-64bcaed30618477286f76cd43f2749f9
Source noteuspto-grants-2014_07