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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3',4-Difluoro-[1,1'-biphenyl]-3-carboxylic acid | HCID 46312332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 2-Fluoro-5-(3-fluorophenyl)-N-(3-methoxyphenyl)benzamide | HCID 89444235 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249085B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-57a0bea7f3b64da4a7bba7e85935a1bf |
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| Source note | uspto-grants-2016_02 |
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