Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (7-Hydroxy-2-benzofuranyl)(5-methyl-3-phenyl-4-isoxazolyl)methanone | HCID 16665213 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 16665215 | HCID 16665215 | 83.6% |
Reaction Steps
To a solution of (7-hydroxy-2-benzofuranyl)(5-methyl-3-phenyl-4-isoxazolyl)methanone (example 4) (100 mg, 0.31 mmol) in THF (3.1 mL) was added ethanol (19 mg, 24 μL, 0.42 mmol) and triphenylphosphine (109 mg, 0.42 mmoL) at room temperature. The resulting mixture was then cooled to 0° C. and diethyl azodicarboxylate (73 mg, 65 μL, 0.42 mmol) added. The resulting mixture was maintained at 0° C. for 30 min and then allowed to warm up to room temperature overnight. The mixture was then adsorbed onto SiO2 and purification by chromatography (SiO2, heptane:ethyl acetate:=100:0 to 75:25) afforded the title compound (90 mg, 83%) as a white solid. MS m/e: 348.4 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07388025B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-0a6090c4503b42ebb0e5f89ff6a31587 |
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| Source note | uspto-grants-2008_06 |
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