HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095927Generated: October 27, 2026
Lithium Hydroxide → 4-{3-Chloro-4-[3,3,3-trifluoro-2-hydroxy-1-methyl-2-(2-methyl-pyridin-4-yl)-propyl]-phenoxymethyl}-benzoic acid
https://huagongshe.com/reaction/1095927
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 4-{3-Chloro-4-[3,3,3-trifluoro-2-hydroxy-1-methyl-2-(2-methyl-pyridin-4-yl)-propyl]-phenoxymethyl}-benzoic acid ethyl ester | HCID 46940643 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 4-{3-Chloro-4-[3,3,3-trifluoro-2-hydroxy-1-methyl-2-(2-methyl-pyridin-4-yl)-propyl]-phenoxymethyl}-benzoic acid | HCID 46940644 | — |
Reaction Steps
4-{3-Chloro-4-[3,3,3-trifluoro-2-hydroxy-1-methyl-2-(2-methyl-pyridin-4-yl)-propyl]-phenoxymethyl}-benzoic acid ethyl ester (250 mg) was dissolved in THF/methanol=5/1 (6 mL) followed by the addition of aqueous LiOH solution (1.0M, 0.54 mL). The mixture was heated to 50° C. for 3.5 hours. The reaction was cooled and concentrated in vacuo. The residue was dissolved in water (5 mL) and aqueous HCl solution (1.0M, 0.54 mL) was added. The mixture was stirred at r.t. for 15 minutes and then at 0° C. for 1 hour. The resulting precipitate was filtered off and washed with cold water. The residual water was removed by co-evaporation with toluene. The resulting solid was dried in vacuo. The title compound was obtained as a colorless solid (220 mg, 93%). MS (m/e)=480.1 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138189B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-3f4698f6137f446a9b1952a18c949c04 |
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| Source note | uspto-grants-2012_03 |
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