HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743519Generated: October 31, 2026
Potassium Carbonate → HCID 86583672, compound
https://huagongshe.com/reaction/1743519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2,4-Dihydroxybenzoate | HCID 16523 | — |
| Reactant | HCID 22237605 | HCID 22237605 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86583672 | HCID 86583672 | 60% |
Reaction Steps
To a solution of N-(8-phenyloctyl)-4-(2-bromo-ethoxy)-3,5-bis(m-trifluoromethylphenyl)benzamide (1.48 g, 2.05 mmol, 1 eq) in acetone (21 mL) was added K2CO3 (1.42 g, 10.25 mmol, 5 eq) and methyl 2,4-dihydroxybenzoate (0.340 g, 2.05 mmol, 1.0 eq). The reaction was heated at reflux for overnight, cooled to rt and concentrated in vacuo. The residue was partitioned between EtOAc and brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography (30% EtOAc:hexane) to afford 2-hydroxy-4-{2-[5′-(8-phenyl-octylcarbamoyl)-3,3″-bis-trifluoromethyl-[1,1′:3′,1″]terphenyl-2′-yloxy]-ethoxy}-benzoic acid methyl ester (0.98 g, 60%) as a colorless oil. 1H NMR (CDCl3) δ 10.90 (s, 1H); 7.92–7.78 (m, 7H); 7.66–7.50 (m, 4H); 7.27–7.12 (m, 5H); 6.18–6.10 (m, 3H); 3.92 (s, 3H); 3.66–3.40 (m, 6H); 2.58 (t, 2H); 1.60 (m, 4H); 1.28 (m, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07008636B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-c5c604c0dd034d73b2a1d3af2cd28b60 |
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| Source note | uspto-grants-2006_03 |
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