HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889752Generated: October 28, 2026
Sodium Hydroxide → 2-{5-[1-(3-Fluoro-5-trifluoromethyl-benzyl)-piperidin-4-yl]-4'-trifluoromethyl-biphenyl-3-yl}-4-methyl-pentanoic acid
https://huagongshe.com/reaction/889752
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-{5-[1-(3-Fluoro-5-trifluoromethyl-benzyl)-piperidin-4-yl]-4'-trifluoromethyl-biphenyl-3-yl}-4-methyl-pentanoic acid ethyl ester | HCID 57666032 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-{5-[1-(3-Fluoro-5-trifluoromethyl-benzyl)-piperidin-4-yl]-4'-trifluoromethyl-biphenyl-3-yl}-4-methyl-pentanoic acid | HCID 25266920 | — |
Reaction Steps
To a solution of a mixture of 2-{5-[1-(3-fluoro-5-trifluoromethyl-benzyl)-piperidin-4-yl]-4′-trifluoromethyl-biphenyl-3-yl}-4-methyl-pentanoic acid ethyl ester and methyl ester (38 mg, 0.06 mmol) in MeOH (1 mL) was added 3N NaOH (0.750 mL) and heated to 60° C. for 2 h. The reaction was concentrated in vacuo to remove MeOH. The thick liquid was acidified to pH=2 by 2N HCl. The resulting acidic solution was extracted with EtOAc. The organic fraction was dried (MgSO4) and concentrated in vacuo. The crude mixture was purified by Gilson reverse phase column chromatography to obtain 2-{5-[1-(3-fluoro-5-trifluoromethyl-benzyl)-piperidin-4-yl]-4′-trifluoromethyl-biphenyl-3-yl}-4-methyl-pentanoic acid. 1H-NMR (MeOD-d4): δ 0.84 (d, 6H), 1.41 (m, 1H), 1.57 (m, 1H), 1.88-1.93 (m, 3H), 2.09 (m, 2H), 2.92 (t, 1H), 3.14 (t, 1H), 3.52 (m, 2H), 3.65 (t, 1H), 4.40 (s, 2H), 7.21 (s, 1H), 7.36 (s, 1H), 7.42 (s, 1H), 7.56-7.69 (m, 7H); Calcd for C32H32F7NO2 (M+H) 596.59, Found 596.40
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252935B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-c62b1b37d1b644a5b6082a6144ac5026 |
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| Source note | uspto-grants-2012_08 |
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