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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398949Generated: October 29, 2026

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

https://huagongshe.com/reaction/1398949

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 numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-ca10df22104d40c29db6c322f0aa5b36
Source noteuspto-grants-2014_12