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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1899590생성일: 2026년 10월 27일

Tetrahydrofuran → 8-Acetyl-2-(dipropylamino)tetralin

https://huagongshe.com/reaction/1899590

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물8-Bromo-2-dipropylamino-1,2,3,4-tetrahydronaphthaleneHCID 14529564—
반응물ButyllithiumHCID 178418339—
생성물Ammonium HydroxideHCID 14923—
생성물8-Acetyl-2-(dipropylamino)tetralinHCID 13227661%

반응 단계

A solution of n-butyllithium (1.6M in hexane, 15.1 ml, 24.2 mmol) was added to a solution of 8-bromo-2-di-n-propylamino-1,2,3,4-tetrahydronaphthalene (5.0 g, 16.1 mmol) in THF (50 ml) at -78° and the reaction stirred at -78° for one hour. Gaseous carbon dioxide was bubbled through the reaction at -78° until the deep violet color which forms dissipates. Methyllithium (1.4M in ether, 23 ml) was added. The reaction was stirred at -78° for 30 minutes and warmed to room temperature. The reaction was stirred for an additional ten minutes at room temperature at which time the pink color had been lost. An additional 10 ml of the methyllithium solution was added and the reaction became pink once again. After 15 minutes, the pink color was lost and an additional 10 ml of the methyllithium solution added. The reaction was poured onto ice, made acidic with hydrochloric acid and extracted with ether. The aqueous layer was made basic and extracted with methylenechloride. The basic extracts were dried (Na2SO4) and concentrated to give 3.8 g of crude product. Purification by flash silica gel chromatography using 2:1 hexane:ether containing trace ammonium hydroxide provided 2-di-n-propylamino-8-acetyl-1,2,3,4-tetrahydronaphthalene as a yellow oil (2.7 g, 61%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05571942
출처 데이터셋uspto-grants-1996_11
ORD IDord-042c270f9fe14a068426cbc88bb28b69
출처 메모uspto-grants-1996_11