Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperonal | HCID 8438 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10679193 | HCID 10679193 | 82% |
Reaction Steps
To a stirred solution of benzo[1,3]dioxole-5-carbaldehyde (657 mg, 4.83 mmol) in methanol (15 mL) was added potassium carbonate (786 mg, 5.69 mmol, 1.3 equiv) and 1-isocyanomethanesulfonyl-4-methyl-benzene (863 mg, 4.38 mmol, 1 equiv). The resulting solution was heated to 70° C. under a nitrogen atmosphere for 3 hours, cooled to ambient temperature, and concentrated in vacuo. The residue was partitioned between methylene chloride and water, and the aqueous layer was extracted three times with methylene chloride. The combined organic layers were dried over sodium sulfate and concentrated in vacuo. Silica gel chromatography (30% ethyl acetate in hexanes) provided 5-benzo[1,3]dioxol-5-yl-oxazole (676 mg, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07273936B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-9185134dfacf4d4c87fec07913a1e7c0 |
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| Source note | uspto-grants-2007_09 |
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