HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolecarboxylate | HCID 17861331 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolylmethanol | HCID 17861205 | 86% |
Reaction Steps
To a solution of methyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolecarboxylate (7.86 g) in tetrahydrofuran (150 ml) was slowly added diisobutylaluminum hydride (1.0 M tetrahydrofuran solution, 60 ml) at 0° C. and the mixture was stirred at room temperature for 30 min. The reaction mixture was poured into dilute hydrochloric acid and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated to give 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolylmethanol (5.93 g, yield 86%) as colorless crystals. The crystals were recrystallized from ethyl acetate-hexane. melting point: 99–100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241785B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-03e9323c091944d498aa4ef128bc9776 |
| Source note | uspto-grants-2007_07 |