HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (5-Tert-butyl-1,2-oxazol-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 5-t-butyl-isoxazole-5-carboxylate | HCID 68779846 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (5-Tert-butyl-1,2-oxazol-3-yl)methanol | HCID 10820794 | — |
Reaction Steps
1.83 g of ethyl 5-t-butyl-isoxazole-5-carboxylate was dissolved in 18 ml of tetrahydrofuran, and 0.70 g of sodium borohydride in 10 ml of ethanol was then added. The mixture was stirred at room temperature for 10 hours. After 5 ml of water was added, the reaction mixture was concentrated to 5 ml under reduced pressure. The concentrated solution was extracted with methyl-t-butyl ether. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to obtain 0.62 g of (5-t-butyl-isoxazol-3-yl)methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846956B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-fdd8deec2e8049fd89820f13d8cb5205 |
| Source note | uspto-grants-2010_12 |