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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771587Generated: November 2, 2026

3-Methoxyaniline → 2-Fluoro-5-(3-fluorophenyl)-N-(3-methoxyphenyl)benzamide

https://huagongshe.com/reaction/1771587

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyanilineHCID 10824—
ReactantPotassium CarbonateHCID 11430—
Reactant3',4-Difluoro-[1,1'-biphenyl]-3-carboxylic acidHCID 46312332—
SolventTetrahydrofuranHCID 8028—
SolventThionyl ChlorideHCID 24386—
Product2-Fluoro-5-(3-fluorophenyl)-N-(3-methoxyphenyl)benzamideHCID 8944423596%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 2-fluoro-5-(3-fluorophenyl)benzoic acid (intermediate III(a)) (500 mg, 2.10 mmol, 1.0 eq) in SOCl2 (5 mL) was heated at 65° C. under N2 for 1 h. The solution was then evaporated in vacuo and the remaining residue dissolved in CH2Cl2 and added dropwise to a mixture of 3-methoxyaniline (220 mg. 1.9 mmol, 0.9 eq) and K2CO3 (1.4 g, 10.1 mmol, 5.0 eq) in THF (10 mL) at 0° C. The reaction was allowed to warm to room temperature and stirred for 2 h. The reaction was quenched with water and the solution extracted with EtOAc. The combined organic extracts were washed with aqueous Na2CO3 and brine, dried (Na2SO4), filtered and evaporated in vacuo to give the title compound as a colourless oil (580 mg, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249085B2
Source datasetuspto-grants-2016_02
ORD IDord-57a0bea7f3b64da4a7bba7e85935a1bf
Source noteuspto-grants-2016_02