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HRID 359853作成日:2026年10月26日

Piperidine → 5-{5-[2-(2-Bromoethenyl)-4-(4,5-dihydro-2-oxazolyl)phenoxy]pentyl}-3-methylisoxazole

https://huagongshe.com/reaction/359853

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物Benzaldehyde, 5-(4,5-dihydro-2-oxazolyl)-2-((5-(3-methyl-5-isoxazolyl)pentyl)oxy)-HCID 5271233—
反応物Triphenylphosphine bromideHCID 22470945—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物5-{5-[2-(2-Bromoethenyl)-4-(4,5-dihydro-2-oxazolyl)phenoxy]pentyl}-3-methylisoxazoleHCID 54238410—

反応手順

To a solution of 1.255 g piperidine in 100 ml ether at 0° under nitrogen was added 12 ml n-butyllithium (1.23 m) followed by 5 g triphenylphosphine bromide. The mixture was then stirred two hours at room temperature and 4.78 g 5-{5-[2-formyl-4-(4,5-dihydro-2-oxazolyl)phenoxy]pentyl}-3-methylisoxazole (Example 70) in 35 ml tetrahydrofuran was added dropwise. The reaction mixture was kept overnight at room temperature and worked up by chromatography to give 0.53 g 5-{5-[2-(2-bromoethenyl)-4-(4,5-dihydro-2-oxazolyl)phenoxy]pentyl}-3-methylisoxazole, colorless needles, m.p. 94°-96° C. after recrystallization from isopropyl acetate and hexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05002960
出典データセットuspto-grants-1991_03
ORD IDord-03bdfa59e2994649a9f6b2c8e9c6b9b0
出典メモuspto-grants-1991_03