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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1804453생성일: 2026년 10월 26일

1-Phenyl-1-hexyne → Methyl 4-butyl-5-phenylisoxazole-3-carboxylate

https://huagongshe.com/reaction/1804453

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenyl-1-hexyneHCID 136908—
반응물Dimethyl nitromalonateHCID 226085—
반응물1-Butyl-3-methylimidazolium hexafluorophosphateHCID 2734174—
용매TolueneHCID 1140—
생성물Methyl 4-butyl-5-phenylisoxazole-3-carboxylateHCID 5853720734.1%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354398B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-4f0dc6e6b8c54f4faab1548759712f2b
출처 메모uspto-grants-2013_01