Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-Phenyl-1-hexyne → Methyl 4-butyl-5-phenylisoxazole-3-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-Phenyl-1-hexyne | HCID 136908 | — |
| 반응물 | Dimethyl nitromalonate | HCID 226085 | — |
| 반응물 | 1-Butyl-3-methylimidazolium hexafluorophosphate | HCID 2734174 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Methyl 4-butyl-5-phenylisoxazole-3-carboxylate | HCID 58537207 | 34.1% |
반응 단계
A solution of hex-1-ynylbenzene (0.274 mL, 1.56 mmol), dimethyl 2-nitromalonate (0.421 mL, 3.12 mmol), 1-butyl-3-methylimidazoliumhexafluorophosphate (0.032 mL, 0.156 mmol) in toluene (6 mL) was subjected to the microwave at 170° C. for 150 min. The reaction mixture was concentrated under reduced pressure, and the residue was purified by flash silica gel chromatography using 5% ethyl acetate in hexane to give methyl 4-butyl-5-phenylisoxazole-3-carboxylate (0.142 g, 0.531 mmol, 34.1% yield) as a clear, colorless oil. The product was 97% pure by HPLC with a ret. time=3.11 min.−Column. CHROMOLITH® SpeedROD 4.6×50 mm (4 min.); Solvent A=10% MeOH, 90% H2O, 0.1% TFA; Solvent B=90% MeOH, 10% H2O, 0.1% TFA. LC/MS M+1=260.2.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08354398B2 |
| 출처 데이터셋 | uspto-grants-2013_01 |
| ORD ID | ord-4f0dc6e6b8c54f4faab1548759712f2b |
| 출처 메모 | uspto-grants-2013_01 |