HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Isoxazolemethanol,5-(trifluoromethyl)-(9CI)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 5-(trifluoromethyl)-3-isoxazolecarboxylate | HCID 66678485 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Isoxazolemethanol,5-(trifluoromethyl)-(9CI) | HCID 15365200 | 96.8% |
Reaction Steps
To a solution of 7.5 g 5-trifluoromethyl-isoxazole-3-carboxylic acid ethyl ester in 85 mL ethanol was added 3.66 g sodium hydride portion wise at RT. The reaction mixture was stirred at RT for 16 h. 100 mL 1M HCl were added drop by drop under ice-bath cooling. The reaction mixture was extracted with 250 mL diethyl ether and 200 mL sat. NaCl solution/water mixture 1:1. The aqueous layer was back-extracted with diethyl ether (2×100 mL). The org. layers were washed with sat. NaCl solution/water mixture 1:1 (2×200 mL). The combined org. layer was dried over Na2SO4, filtered off and concentrated in vacuo to yield 5.8 g of the title compound as brown oil. MS (EI): 167 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08729105B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-30fdb0c6029840dcabe3bb5268e6af88 |
| Source note | uspto-grants-2014_05 |