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HRID 1760063作成日:2026年10月25日

Ammonia → 1-(8-Quinolyl)-2,3-dimethylcyclopentadiene

https://huagongshe.com/reaction/1760063

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-Cyclopenten-1-one, 2,3-dimethyl-HCID 14270—
反応物8-BromoquinolineHCID 140109—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(8-Quinolyl)-2,3-dimethylcyclopentadieneHCID 2235212441.4%

反応手順

5 ml of n-BuLi (2.5 M in hexane, 12.5 mmol) were added dropwise at −95° C. to a solution of 2.5 g of 8-bromoquinoline (12 mmol) in 120 ml of THF, the mixture was stirred for 15 minutes, and 1.3 g of 2,3-dimethylcyclopent-2-enone (12 mmol) dissolved in 10 ml of THF were subsequently added. After warming to room temperature, the solution was refluxed for one hour. The cooled reaction mixture was hydrolyzed using ice, acidified using hydrochloric acid and then neutralized using ammonia solution. The aqueous phase was extracted with diethyl ether, and the combined organic phases were dried. Distillation at 150° C./0.05 mbar gave 1.1 g of 1-(8-quinolyl)-2,3-dimethylcyclopentadiene (40%) as a yellow, viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06838563B2
出典データセットuspto-grants-2005_01
ORD IDord-93bae73bc48f4aecbc945eee11b3dff5
出典メモuspto-grants-2005_01