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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373194Generated: November 1, 2026

Dimethyl Sulfate → Methyl 3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)-5-nitrobenzoate

https://huagongshe.com/reaction/1373194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantHexaneHCID 8058—
ReactantSodium BicarbonateHCID 516892—
Reactant3,4-Difluoro-2-(2-fluoro-4-iodophenylamino)-5-nitrobenzoic acidHCID 21074292—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)-5-nitrobenzoateHCID 58781115—

Reaction Steps

To a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-nitro-benzoic acid (595.3 g, 1.363 mol) in acetone (9 L) was added sodium bicarbonate (609.0 g, 3.48 mol) and the mixture was stirred for 10 min. To this suspension was added dimethylsulfate (285.6 ml, 3.026 mol) and refluxed for 3 h (completion of reaction was confirmed by TLC-hexane: EtOAc/4:1), cooled to room temperature and evaporated under vacuum. The residue (yellow) was further digested in hot methanol (2 L), filtered, washed with methanol and dried to give the title compound as a solid (yellow). Yield: 405.63g (65.54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160915B2
Source datasetuspto-grants-2007_01
ORD IDord-558c4bb42bc54c82a1524ebc74602d7d
Source noteuspto-grants-2007_01