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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705408Generated: October 29, 2026

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

https://huagongshe.com/reaction/705408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1,2,3,5-Tetrafluoro-4-nitrobenzeneHCID 67566—
Reactant2-Fluoro-4-iodoanilineHCID 185694—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
Product2,3,5-trifluoro-N-(2-fluoro-4-iodophenyl)-6-nitroanilineHCID 5743007259.24%

Reaction Steps

A solution of 1.0 M lithium hexa methyl disilazide (LiN(SiMe3)2) “LHMDS” (15.37 mL, 15.37 mmol) was slowly added to a stirred solution of 2-fluoro-4-iodoaniline (3.64 g, 15.37 mmol) in dry THF (100 mL) under nitrogen at −78° C. and stirring continued at −78° C. for another hour. 2,3,4,6-Tetrafluoronitrobenzene was added, and the reaction mixture was allowed to warm to room temperature and stirring continued for another 16 hours. Ethyl acetate (200 mL) was added and the organic phase was washed with water, dried over sodium sulfate and further purified by column chromatography to provide the product as a yellow solid (3.75 g, 59.24%). M−H+: 410.9. 1H NMR (DMSO, 300 MHz): 6.85 (t, 1H); 7.38 (d, 1H); 7.62 (m, 2H); 8.78 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174933B2
Source datasetuspto-grants-2015_11
ORD IDord-b19edaa4fd7b4e3badd48569db582a45
Source noteuspto-grants-2015_11