Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | HCID 66928589 | HCID 66928589 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 66928768 | HCID 66928768 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and a Dean-Stark apparatus under inert atmosphere (N2), a solution of 1-[5-(4-nitro-pyrazol-1-ylmethyl)-isoxazol-3-yl]-ethanone (336 mg, 1.42 mmol) in ethylene glycol (1.59 mL, 28.45 mmol) was treated with trimethylorthoformate (0.31 mL, 2.84 mmol) followed by LiBF4 (27 mg, 0.29 mmol). The reaction mixture was heated at 95° C. overnight. Sat. aq. NaHCO3 (10 mL) was added and the mixture was extracted with EA (10 mL). The org. extracts were washed with brine (2×20 mL), dried over MgSO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:10 hept-EA) gave the title compound as a yellow oil. TLC: rf (20:10 hept-EA)=0.19. LC-MS-conditions 02: tR=0.86 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288419B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-15d89d3785024000a486a6ec5717a91a |
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| Source note | uspto-grants-2012_10 |
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