HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349217Generated: November 1, 2026
Sodium Acetate → {2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-yl}-methanol
https://huagongshe.com/reaction/349217
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Chloromethyl-2-[2-(4-trifluoromethoxy-phenyl)-vinyl]-oxazole | HCID 69071577 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | {2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-yl}-methanol | HCID 68934459 | — |
Reaction Steps
A solution of 4-chloromethyl-2-[2-(4-trifluoromethoxy-phenyl)-vinyl]-oxazole (0.300 g, 0.99 mmol) and sodium acetate (0.162 g, 1.976 mmol) in acetic acid (5 ml) is refluxed for 48 h. The reaction mixture is cooled to r.t., concentrated in vacuo and the resulting residue is dissolved in ethanol (2 ml) and 5M potassium hydroxide (KOH) (5 ml). The solution is refluxed for 5 h and cooled to r.t. Saturated ammonium chloride (NH4Cl) is added and the mixture is extracted with ethyl acetate (3×). The extract is washed with brine, dried over Na2SO4 and concentrated in vacuo. The crude product is purified by flash column chromatography (ethyl acetate/hexanes 1:1) yielding {2-[2-(4-Trifluoromethoxy-phenyl)-vinyl]-oxazol-4-yl}-methanol as a colorless solid. Yield 200 mg (71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179812B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-32a4d2210f884489a89d3abd11ec2065 |
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| Source note | uspto-grants-2007_02 |
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