Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-(Benzo[d]oxazol-2-yl)-N,N-dimethylethenamine | HCID 14972993 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Benzoxazole-2-carbaldehyde | HCID 4483393 | — |
Reaction Steps
To (E)-2-(benzo[d]oxazol-2-yl)-N,N-dimethylethenamine (1 g, 5.32 mmol) in THF (15 mL) at 0° C. was added water (15 mL) and NaIO4 (3.4 g, 16 mmol). The resulting mixture was stirred at 0° C. for 10 min, then at room temperature for 2 h. To the solution was added H2O and EtOAc and then the mixture was filtered. The clear solution was extracted with EtOAc and the organic phase was washed with aqueous NaHCO3 solution. The organic phase was concentrated and the residue was purified by column chromatography to give the title compound (120 mg). MS (ESI) m/z 148 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969349B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-605ba309bf5647b7a7231e7cfb5ee0d1 |
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| Source note | uspto-grants-2015_03 |
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