HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288959Generated: October 30, 2026
2,2,2-Trifluoroethanol → 1-{4-[5-Phenyl-4-(2,2,2-trifluoroethoxymethyl)-oxazol-2-yl]-piperidin-1-yl}-ethanone
https://huagongshe.com/reaction/2288959
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-[4-(4-Chloromethyl-5-phenyl-oxazol-2-yl)-piperidin-1-yl]ethanone | HCID 18700436 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-{4-[5-Phenyl-4-(2,2,2-trifluoroethoxymethyl)-oxazol-2-yl]-piperidin-1-yl}-ethanone | HCID 18700439 | — |
Reaction Steps
A solution of 1-[4-(4-chloromethyl-5-phenyl-oxazol-2-yl)-piperidin-1-yl]ethanone (30 g, 94.1 mmol), prepared as in Intermediate 3B, in 2,2,2-trifluoroethanol (450 ml) is treated with a solution of NaOH (56 g, 1412 mmol) in water (150 ml). After heating at 72° C. for 15 hours, the reaction mixture is concentrated. The residue is partitioned between EtOAc and water. The aqueous phase is reextracted once with EtOAc, and the combined organic phases are washed with saturated brine, dried (Na2SO4) and concentrated to afford 1-{4-[5-phenyl-4-(2,2,2-trifluoroethoxymethyl)-oxazol-2-yl]-piperidin-1-yl}-ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090825 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-7e623cfd335e4f6d8e6ec1f823c663cb |
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| Source note | uspto-grants-2000_07 |
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