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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240984Generated: October 30, 2026

Ethyl Acetate → 2,3-Difluoro-N-(2-fluoro-4-iodophenyl)-5-methoxy-6-nitroaniline

https://huagongshe.com/reaction/240984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium MethoxideHCID 10942334—
Reactant2,3,5-trifluoro-N-(2-fluoro-4-iodophenyl)-6-nitroanilineHCID 57430072—
SolventTetrahydrofuranHCID 8028—
Product2,3-Difluoro-N-(2-fluoro-4-iodophenyl)-5-methoxy-6-nitroanilineHCID 5938631247.6%

Reaction Steps

A stirred solution of (2-fluoro-4-iodo-phenyl)-(2,3,5-trifluoro-6-nitro-phenyl)-amine (1.23 g, 3 mmol) in dry THF (25 ml) under nitrogen was cooled to −78° C. and a solution of 25% sodium methoxide (0.68 ml, 0.3 mmol) was added slowly. The reaction mixture was allowed to warm to room temperature and stirring continued for another 16 hours. TLC indicated incomplete reaction. Ethyl acetate (100 mL) was added to the reaction mixture and the organic layer was washed with water, dried over sodium sulfate and further purified by column chromatography to provide the desired compound as a yellow solid (0.6 g, 47.6%). m/z=424 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648116B2
Source datasetuspto-grants-2014_02
ORD IDord-4ca59364f5384164adcf00cb0acae9fe
Source noteuspto-grants-2014_02