HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-(4-Fluoro-phenyl)-5-((E)-styryl)-isoxazole-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 3-(4-fluorophenyl)-5-methyl-1,2-oxazole-4-carboxylate | HCID 22309061 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-Fluoro-phenyl)-5-((E)-styryl)-isoxazole-4-carboxylic acid | HCID 66643836 | 77% |
Reaction Steps
To a solution of 3-(4-fluoro-phenyl)-5-methyl-isoxazole-4-carboxylic acid ethyl ester (20.0 g, 80.2 mmol) and benzaldehyde (8.19 mL, 80.2 mmol) in ethanol (113 mL) was added sodium ethoxide (2.71 M, 32.5 mL, 88.3 mmol) and the reaction mixture was heated under reflux for 1 h. Hydrochloric acid (1 N, 96.3 mL) was added and the resulting mixture was extracted with toluene. The solvent was then distilled off to afford the title compound (19.1 g, 77%) as a light yellow solid. MS: m/e=308.0 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173652B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-b1d95cc8e0a14beea56617d090d80692 |
| Source note | uspto-grants-2012_05 |