Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2-Amino-2-methyl-1-propanol | HCID 11807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 10511031 | HCID 10511031 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21251137 | HCID 21251137 | 52.2% |
Reaction Steps
3-Ethoxy-4-methylisoxazole-5-carbonitrile (2.6 g, 17.1 mmol), 5.4 M NaOMe in MeOH (0.6 mL, 3.4 mmol) and EtOH (80 mL) was stirred at room temperature for 30 min. Acetic acid (2.2 mL, 39.3 mmol) and 2-amino-2-methylpropan-1-ol (1.8 mL, 18.8 mmol) were added, and the resulting mixture was boiled under reflux for 20 h. The reaction mixture was cooled, added water (100 mL) and extracted with EtOAc (3×100 mL). The organic extracts were washed with 1 M NaOH (50 mL), brine, dried (MgSO4) and evaporated in vacuo. The residue was dissolved in EtOH (60 mL), a solution of KOH (1.8 g, 32 mmol) in water (12 mL) was added, and the mixture was stirred at room temperature for 20 h. EtOH was removed in vacuo, water was added (80 mL) and the aqueous phase extracted with EtOAc (3×100 mL). The organic extracts were washed with brine, dried (MgSO4) and evaporated in vacuo. Flash chromatography (silica gel, eluent: EtOAc/heptane/triethylamine=75:25:1) gave crude title compound as a yellow oil (2.0 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06200999B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-0e5c8d596fc84607891526ab4678cbf4 |
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| Source note | uspto-grants-2001_03 |
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