HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl-t-butylacetylene → Methyl 4-tert-butyl-5-phenylisoxazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl-t-butylacetylene | HCID 138165 | — |
| Reactant | Dimethyl nitromalonate | HCID 226085 | — |
| Solvent | Mesitylene | HCID 7947 | — |
| Product | Methyl 4-tert-butyl-5-phenylisoxazole-3-carboxylate | HCID 58537183 | 15.4% |
Reaction Steps
A solution of (3,3-Dimethylbut-1-ynyl)benzene (400 mg, 2.53 mmol) and dimethyl nitromalonate (0.853 mL, 6.32 mmol) in mesitylene (5 mL) was heated at 150° C. for 48 h. The reaction mixture was concentrated, and the residue was purified by silica gel chromatography with hexanes/ethyl acetate (10/1) to yield methyl 4-tert-butyl-5-phenylisoxazole-3-carboxylate (101 mg). The compound had an HPLC ret. time=3.39 min.−Column. YMC S5 COMBISCREEN® 4.6×50 mm; Gradient time: 4 min; Flow rate=4 ml/min; Solvent A=10% MeOH−90% Water−0.2% H3PO4; Solvent B=90% MeOH−10% water−0.2% H3PO4; Start % B=0; Final % B=100. LC-MS: M+1=260+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354398B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-8306893196d84c0e85da5b01c4b0e7ec |
| Source note | uspto-grants-2013_01 |