Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Isoxazole | HCID 9254 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,2-Benzisoxazole | HCID 71073 | — |
Reaction Steps
To a 100 L cylindrical vessel with heating coils were charged EtOAc (20 L) and TsOH/H2O (2.304 kg, 12.11 mol), and the mixture was heated to 35-45° C. to dissolve. The acid solution was fed into the isoxazole batch with further distilling, maintaining a constant volume of 25 L. An additional 20 L of EtOAc was distilled to azeotropically dry the mixture. A slurry began to form, and it continued to thicken on addition and concentration. The final KF was 400 ppm water. The batch was heated to 60° C. and allowed to slowly cool to ambient temperature overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834036B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-97e4c6bae3a24059a274446ecaad8738 |
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| Source note | uspto-grants-2010_11 |
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