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HRID 896737作成日:2026年10月26日

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

https://huagongshe.com/reaction/896737

反応式

関与物質

役割名称HCID仕込み量
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 2235212960.7%

反応手順

A solution of 4.4 g 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) was added dropwise while stirring. After ten minutes of stirring, 3.5 g of 2,3,4,5-tetramethylcyclopentenone (25 mmol) was added dropwise; the solution was heated to room temperature and then heated in reflux for one hour. The solution was cooled down; ice and hydrochloric acid to approximately pH 1 were added; and after neutralization with ammonia solution, the phases were separated and the aqueous phase was extracted with pentane. The combined organic extracts were dried, the pentane was removed in a vacuum, and the remaining brown oil was distilled in a high vacuum (boiling point: 115° C. at 0.01 mbar). A 60% yield (3.2 g) of 1-(2-methyl-8-quinolyl)-2,3,4,5-tetramethylcyclopentadiene in the form of yellow, viscous oil was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06919412B1
出典データセットuspto-grants-2005_07
ORD IDord-dd7731bab6ef4a2db1c22a813597413c
出典メモuspto-grants-2005_07