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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470367Generated: October 29, 2026

Ethyl bromodifluoroacetate → (4-Amino-3-methyl-5-nitro-phenyl)-difluoro-acetic acid ethyl ester

https://huagongshe.com/reaction/470367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromodifluoroacetateHCID 69585—
Reactant4-Iodo-2-methyl-6-nitroanilineHCID 24899646—
CatalystCopperHCID 23978—
SolventDimethyl SulfoxideHCID 679—
Product(4-Amino-3-methyl-5-nitro-phenyl)-difluoro-acetic acid ethyl esterHCID 5978432065.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-iodo-2-methyl-6-nitroaniline (2.78 g, 10 mmol) and 2-bromo-2,2-difluoroacetic acid ethyl ester (2.03 g, 10 mmol) in anhydrous DMSO (20 mL) was added copper powder (1.28 g, 20 mmol). The mixture was purged with N2 and heated at 60° C. in a sealed vial for 14 h. After being cooled to the room temperature, the reaction mixture was poured into 20% aqueous NH4Cl solution (300 mL). The resulting mixture was basified to pHY=8.5 with saturated aqueous Na2CO3 solution and was extracted with EtOAc (3×100 mL). The organic extract was washed with brine (2×30 mL), dried over Na2SO4 and concentrated. The residue was purified by chromatography (40:1 hexanes/EtOAc) to afford the title compound (1.79 g, 65%). 1H NMR (CDCl3) δ 1.36 (t, 3H), 2.30 (s, 3H), 4.36 (q, 2H), 6.41 (br s, 2H NH), 7.51 (s, 1H), 8.33 (s, 1H). ESI-MS m/z 275 (MH+), 255 (M-F)+, 297 (M+Na)+, 549 (2M+1)+ and 571 (2M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629147B2
Source datasetuspto-grants-2014_01
ORD IDord-51d97dab3a644cb8bf9d3af9708dd9a8
Source noteuspto-grants-2014_01