HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-Phenylisoxazole-5-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Phenylisoxazole-5-carboxylic Acid | HCID 737474 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Phenylisoxazole-5-carbonyl chloride | HCID 14397324 | — |
Reaction Steps
Added to 500 g (4.2 mol) of thionyl chloride were 110 g (0.58 mol) of 3-phenylisoxazole-5-carboxylic acid prepared above in the procedure (2), followed by the further addition of 2 ml of dimethylformamide. The resulting mixture was heated under reflux for 3 hours. After completion of the reaction, thionyl chloride was distilled off under reduced pressure, followed by the addition of 500 ml of benzene. When the mixture thus obtained was distilled under reduced pressure, the title compound, i.e., 3-phenylisoxazole-5-carboxylic acid chloride was obtained as a solid. It was provided for the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05498619 |
| Source dataset | uspto-grants-1996_03 |
| ORD ID | ord-61104968dbd645a0bdcc41a461a628b0 |
| Source note | uspto-grants-1996_03 |