HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548198Generated: October 29, 2026
Sodium Hydroxide → 4-(3,5-Bis(trifluoromethyl)benzyloxy)-3-phenylbutanoic acid
https://huagongshe.com/reaction/548198
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoate | HCID 86624037 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(3,5-Bis(trifluoromethyl)benzyloxy)-3-phenylbutanoic acid | HCID 86624038 | 109.1% |
Reaction Steps
Ethyl 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoate (26.06 g, 60 mmol) was dissolved in ethanol (300 mL), a 2 mol/L aqueous solution of sodium hydroxide was added thereto and the mixture was stirred for 20 hours at room temperature. The solvent was evaporated in vacuo and the resulting residue was dissolved in water and acidified with 6 mol/L hydrochloric acid. The oily product separated out therefrom was extracted with chloroform and the organic layers were combined and washed with water and a saturated saline solution. After it was dried over anhydrous sodium sulfate, the solvent was evaporated in vacuo to give 4-(3,5-bis(trifluoromethyl)benzyloxy)-3-phenylbutanoic acid (26.60 g, 90%) as an oily product. 1H-NMR (DMSO-d6) δ: 2.56 (dd, J=8.4, 16.0 Hz, 1H), 2.73 (dd, J=6.4, 16.0 Hz, 1H), 3.35-3.40 (m, 1H), 3.63-3.66 (m, 2H), 4.64 and 4.66 (ABq, J=13.4 Hz, 2H), 7.19-7.25 (m, 1H), 7.27-7.31 (m, 4H), 7.88 (s, 2H), 7.98 (s, 1H), 12.09 (brs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07939552B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-15bd7307ac574a6c814ce9446a0d1a27 |
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| Source note | uspto-grants-2011_05 |
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