HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269566Generated: October 25, 2026
Potassium Carbonate → Methyl 4-(acetylamino)-2''-{[(2, 4-difluorophenyl)methyl]oxy}-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-2-carboxylate
https://huagongshe.com/reaction/269566
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2,4-Difluorobenzyloxy)-5-trifluoromethylphenylboronic acid | HCID 21112905 | — |
| Reactant | Toluene ethanol | HCID 21863594 | — |
| Reactant | Methyl 4-(acetylamino)-2'-bromo-2-biphenylcarboxylate | HCID 58731002 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 4-(acetylamino)-2''-{[(2, 4-difluorophenyl)methyl]oxy}-5''-(trifluoromethyl)-1,1':2',1''-terphenyl-2-carboxylate | HCID 58731000 | — |
Reaction Steps
A mixture of 2-[(2,4-difluorobenzyl)oxy]-5-trifluoromethylbenzene boronic acid (66 mg, 0.2 mmol), methyl 4-(acetylamino)-2′-bromo-2-biphenylcarboxylate (110 mg, 0.32 mmol), potassium carbonate (138 mg, 1 mmol) and tetrakis(triphenylphosphine)palladium(0) (23 mg, 5 mol %) in 1:1 toluene/ethanol (4 ml) was stirred and heated at 90° C. under nitrogen for 2 hours. After cooling the mixture was diluted with diethyl ether and water and the organic phase dried (MgSO4) and evaporated to dryness. The residue was chromatographed with ethyl acetate/iso-hexane (2:3) to yield the title compound as a pale yellow gum. (90 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446222B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-2c3b5cb6f228406ab194bb627af8d4be |
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| Source note | uspto-grants-2008_11 |
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