HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 5-methyl-3-phenylisoxazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 5-Methyl-3-phenylisoxazole-4-carboxylic acid | HCID 14343 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | Ethyl 5-methyl-3-phenylisoxazole-4-carboxylate | HCID 70838 | — |
Reaction Steps
A mixture of 5-methyl-3-phenyl-isoxazole-4-carboxylic acid (10.0 g, 0.05 mol) and thionyl chloride (18.0 ml, 0.25 mol) in ethanol (100 ml) was refluxed for 5 h before it was cooled to room temperature and concentrated in vacuo. The residue was partitioned between ethyl acetate and water, the organic layer was washed with saturated aqueous sodium bicarbonate solution, and brine, before it was dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound as a yellow solid (10.24 g): 1H NMR (CDCl3, 200 MHz): δ=7.61 (m, 2H), 7.43 (m, 3H), 4.25 (q, J=7.0 Hz, 2H), 2.73 (s, 3H), 1.23 (t, J=7.0 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08269008B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-07b71e6733c74e4aa4e89b177b266bf0 |
| Source note | uspto-grants-2012_09 |