HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Methyl 3-(5-p-tolylisoxazol-3-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Ethynyltoluene | HCID 13018 | — |
| Reactant | Methyl 3-[chloro(hydroxyimino)methyl]benzoate | HCID 85867392 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Methyl 3-(5-p-tolylisoxazol-3-yl)benzoate | HCID 57907091 | — |
Reaction Steps
In a 25 ml round flask, 1.9 g (8.9 mmol) of 3-[chloro-(hydroxyimino)-methyl]-benzoic acid methyl ester and 1.03 g (8.9 mmol) of 1-ethynyl-4-methyl-benzene are dissolved in 12 ml of CHCl3 at 0° C. To this solution, 36 μl (0.4 mmol, 0.05 eq.) of pyridine and subsequently 1.24 ml (8.9 mmol) of triethyl amine are added and the mixture is stirred under warming to room temperature for 2 h. Then, the mixture is poured onto water, extracted twice with CH2Cl2, the organic layers are dried with brine and Na2SO4 and then concentrated. Chromatographic purification (250 g SiO2; gradient elution, eluent: hexane/ethyl acetate 95:5→9:1) yields the title compound as a white solid. Mass spectrum: m/z (M+H)+: 294.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432293B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-6021b36f6361478ba2cfafada77afcf8 |
| Source note | uspto-grants-2008_10 |