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HRID 47837作成日:2026年10月25日

Ammonia → 1-(2-Methyl-8-quinolyl)-2,3,4,5-tetramethylcyclopentadiene

https://huagongshe.com/reaction/47837

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Hydrochloric AcidHCID 313—
反応物2,3,4,5-Tetramethyl-2-cyclopentenoneHCID 41092—
反応物8-Bromo-2-methylquinolineHCID 4715030—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-Methyl-8-quinolyl)-2,3,4,5-tetramethylcyclopentadieneHCID 2235212960%

反応手順

A solution of 4.4 q of 8-bromo-2-methylquinoline (20 mmol) in 50 ml of THF was cooled to −78° C., and 8.8 ml of n-BuLi (2.5 M in hexane, 22 mmol) were added dropwise with stirring. After the mixture had been stirred for 10 minutes, 3.5 g of 2,3,4,5-tetramethylcyclopentenone (25 mmol) were added dropwise, and the solution was warmed to room temperature, refluxed for one hour and cooled. Ice and hydrochloric acid were added to about pH 1, the mixture was neutralized using ammonia solution, the phases were separated, and the aqueous phase was extracted with pentane. After the combined organic extracts had been dried, the pentane was removed under reduced pressure, and the brown oil which remained was distilled under a high vacuum (b.p.: 115° C./0.01 mbar). 1-(2-Methyl-8-quinolyl)-2,3,4,5-tetramethylcyclopentadiene was obtained as a yellow, viscous oil in a yield of 60% (3.2 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699948B2
出典データセットuspto-grants-2004_03
ORD IDord-5527d22d37c34191bd0646c414eafd1c
出典メモuspto-grants-2004_03