HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427875Generated: November 2, 2026
Citric Acid → 2-[2-(4-Fluoro-phenyl)-6-(4-trifluoromethyl-phenyl)-pyridin-4-yl]-4-methyl-pentanoic acid
https://huagongshe.com/reaction/2427875
Participants
| Role | Name | HCID | Charge |
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| Reactant | Citric Acid | HCID 311 | — |
| Reactant | 2-[2-(4-Fluoro-phenyl)-6-(4-trifluoromethyl-phenyl)-pyridin-4-yl]-4-methyl-pentanoic acid methyl ester | HCID 59161708 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-[2-(4-Fluoro-phenyl)-6-(4-trifluoromethyl-phenyl)-pyridin-4-yl]-4-methyl-pentanoic acid | HCID 45108076 | 77.3% |
Reaction Steps
A solution of 2-[2-(4-fluoro-phenyl)-6-(4-trifluoromethyl-phenyl)-pyridin-4-yl]-4-methyl-pentanoic acid methyl ester (80 mg, 0.18 mmol) in NaOH (1N, 1 mL) and THF (4 mL) was stirred at 40° C. overnight. The mixture was cooled to room temperature, acidified with 10% citric acid, and extracted with CH2Cl2 (3×). The organic layer was washed with brine, dried over Na2SO4, filtered and evaporated. The residue was purified by chromatography (5-25% ethyl acetate in CH2Cl2) to give the product as a white foam (60 mg, 77%). 1H NMR (300 MHz, CDCl3) δ 8.21 (d, J=8.29 Hz, 2H), 8.05-8.15 (m, 2H), 7.73 (d, J=8.29 Hz, 2H), 7.65 (d, J=1.51 Hz, 2H), 7.11-7.23 (m, 2H), 3.80 (t, J=7.72 Hz, 1H), 2.08-2.16 (m, 1H), 1.77 (dt, J=7.06, 13.75 Hz, 1H), 1.48-1.64 (m, 1H), 0.96 (d, J=6.40 Hz, 6H). MS m/e 432.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968725B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-6bc6aa31e9434a3e8c3ff1608fa8a342 |
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| Source note | uspto-grants-2011_06 |
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