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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1440331생성일: 2026년 10월 23일

Sulfuric Acid → 3-(4-Methylphenyl)-5-butyrylisoxazole

https://huagongshe.com/ko/reaction/1440331

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물Ethylmalonic acidHCID 11756—
반응물Sodium hydrideHCID 24758—
반응물EthylpropanedioateHCID 6950106—
반응물Dipyranyl ethylmalonateHCID 19976934—
반응물3-(4-Methylphenyl)isoxazole-5-carboxylic acid chlorideHCID 53715915—
반응물Sodium dipyranyl malonateHCID 67715643—
용매Acetic AcidHCID 176—
용매BenzeneHCID 241—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물3-(4-Methylphenyl)-5-butyrylisoxazoleHCID 19976953—

반응 단계

In 50 ml of benzene, 2.6 g (57.5 mmol) of 60% sodium hydride were added to dipyranyl ethylmalonate which had been prepared from 5.7 g (43.2 mmol) of ethylmalonic acid, 9.0 g (107.1 mmol) of 3,4-dihydropyran and 1 droplet of concentrated sulfuric acid. At 40°-50° C., the ethylmalonate was converted to sodium dipyranyl malonate, to which a tetrahydrofuran solution of 3-(4-methylphenyl)isoxazole-5-carboxylic acid chloride synthesized above in the procedure (3) was added dropwise at room temperature. They were reacted for 3 hours. The reaction mixture was added with 10 ml of acetic acid and then heated under reflux for 6 hours. The mixture thus obtained was added into water and then extracted with benzene. The benzene extract was washed successively with an aqueous solution of sodium hydrogencarbonate and water. The organic layer was dried over anhydrous sodium sulfate and the solvent was distilled off. Hexane was added to the residue, and 3-(4-methylphenyl)-5-butyrylisoxazole precipitated as crystals was collected by filtration.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05498619
출처 데이터셋uspto-grants-1996_03
ORD IDord-373eee14e52f4e4fbf79c7abb5aecdde
출처 메모uspto-grants-1996_03