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HRID 1440328作成日:2026年10月26日

Sulfuric Acid → Dipyranyl ethylmalonate

https://huagongshe.com/reaction/1440328

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物3,4-dihydro-2H-pyranHCID 8080—
反応物Ethylmalonic acidHCID 11756—
反応物Sodium hydrideHCID 24758—
反応物3-Phenylisoxazole-5-carbonyl chlorideHCID 14397324—
溶媒Acetic AcidHCID 176—
溶媒BenzeneHCID 241—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Dipyranyl ethylmalonateHCID 19976934—

反応条件

温度50 °C

反応手順

To 130 ml of benzene, were added 12.9 g (97.7 mmol) of ethylmalonic acid, 20.2 g (240.5 mmol) of 3,4-dihydropyran and 2 droplets of concentrated sulfuric acid. They were reacted for 1 hour under ice cooling, whereby dipyranyl ethylmalonate was prepared. The reaction mixture was added with 4.7 g (117.5 mmol) of 60% sodium hydride, followed by heating under stirring at 50° C. for 5 hours. A solution of 15.0 g (79.4 mmol) of 3-phenylisoxazole-5-carboxylic acid chloride, which had been synthesized above in the procedure (3), in 70 ml of tetrahydrofuran was added under ice cooling to the above-prepared reaction mixture. The mixture thus obtained was then subjected to a reaction at room temperature for 12 hours. The reaction mixture was added with 20 ml of acetic acid and then heated under reflux for 8 hours. The reaction mixture so obtained was poured into water and then extracted with benzene. The organic layer was washed successively with water, an aqueous solution of sodium hydrogen-carbonate and saturated saline, and was then dried over anhydrous sodium sulfate. After the benzene was distilled off, hexane was added into the residue. Crystals precipitated was collected by filtration, so that 3-phenyl-5-butyrylisoxazole was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05498619
出典データセットuspto-grants-1996_03
ORD IDord-0d78b119af5a4258982a5e9f024e3796
出典メモuspto-grants-1996_03