돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1760067생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1760067

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Hydrochloric AcidHCID 313—
반응물2,3,4,5-Tetramethyl-2-cyclopentenoneHCID 41092—
반응물8-Bromo-2-methylquinolineHCID 4715030—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-(2-Methyl-8-quinolyl)-2,3,4,5-tetramethylcyclopentadieneHCID 2235212960%

반응 단계

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) 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06838563B2
출처 데이터셋uspto-grants-2005_01
ORD IDord-57282727f02d42d793c1cff2cd7b5ad4
출처 메모uspto-grants-2005_01