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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161830Generated: October 29, 2026

2-Fluoroaniline → 5-Bromo-3,4-difluoro-2-((2-fluorophenyl)amino)benzoic acid

https://huagongshe.com/reaction/1161830

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroanilineHCID 9584—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant5-Bromo-2,3,4-trifluorobenzoic acidHCID 11118637—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-3,4-difluoro-2-((2-fluorophenyl)amino)benzoic acidHCID 5951938872%

Reaction Steps

To a solution of 2-fluoro-aniline (177 mmol, 17.0 ml) in THF (80 mL) at −78° C. was added LiHMDS (265 mmol, 265 ml) and stirred for 30 min. To the reaction was added a solution of 5-bromo-2,3,4-trifluorobenzoic acid (78.4 mmol, 20.1 g) in THF (60 ml) at −78° C. The reaction was warmed to room temperature and stirred at the temperature over night. The reaction is concentrated and slowly 10% HCl (180 ml) is added. The mixture was extracted with ethyl acetate (100 ml×3), dried over MgSO4 and concentrated under reduced pressure. The crude material was taken in CH2Cl2 (−250 ml) and heated up to 45° C. for 10 min. Purification by trituration with CH2Cl2 gave 11 g (72%) of the desired product as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820664B2
Source datasetuspto-grants-2010_10
ORD IDord-52e5fa1ca882466dbba5313ea7aa9a97
Source noteuspto-grants-2010_10