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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288638Generated: November 2, 2026

Ethyl 2-chloro-4-fluoro-5-nitrobenzoate → Ethyl 5-amino-2-chloro-4-fluorobenzoate

https://huagongshe.com/reaction/2288638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloro-4-fluoro-5-nitrobenzoateHCID 22508453—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-amino-2-chloro-4-fluorobenzoateHCID 2250846190%

Reaction Conditions

Temperature40 °C

Reaction Steps

Then, 60 g of iron powder and 500 ml of 10% acetic acid were mixed, and the mixture was heated to 40° C. Separately, 50 g (0.20 mol) of ethyl 2-chloro-4-fluoro-5-nitrobenzoate was dissolved in a mixed solution of 20 ml of acetic acid and 20 ml of ethyl acetate, and added dropwise to the above iron powder-acetic acid mixed solution. Then, the reaction mixture was stirred at 50° C. for 1 hour and filtered though celite. The filtrate was extracted with 100 ml of ethyl acetate. The ethyl acetate layer was washed with aqueous sodium bicarbonate solution and saturated sodium chloride solution, and dried with magnesium sulfate. The solvent was distilled out, and the residue was purified by silica gel chromatography, which afforded to 40 g (0.18 mol) of ethyl 5-amino-2-chloro-4-fluorobenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090753
Source datasetuspto-grants-2000_07
ORD IDord-78ba8855c4f749329bf8ab3ad625bada
Source noteuspto-grants-2000_07