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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22139생성일: 2026년 10월 25일

Water → 2-Di-n-propylamino-8-(quinol-2-yl)-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/22139

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-ChloroquinolineHCID 11928—
반응물MagnesiumHCID 5462224—
반응물8-Bromo-2-dipropylamino-1,2,3,4-tetrahydronaphthaleneHCID 14529564—
촉매1,2-DibromoethaneHCID 7839—
용매TetrahydrofuranHCID 8028—
생성물2-Di-n-propylamino-8-(quinol-2-yl)-1,2,3,4-tetrahydronaphthaleneHCID 23373524181.9%

반응 단계

2-Di-n-propylamino-8-bromo-1,2,3,4-tetrahydronaphthalene (1 g, 3.22 mmol) was added to a refluxing mixture of magnesium turnings (120 mg, 4.9 mmol) in 50 ml THF. Formation of the Grignard reagent was initiated by addition of 0.2 ml 1,2-dibromoethane (0.002 mmol). After 1.5 hours, 220 mg (0.33 mmol) Ni[PPh3 ]2Cl2 in 10 ml of THF were added followed by 800 mg (4.89 mmol) of 2-chloroquinoline. The solution continued to reflux for 15 minutes after which it was cooled, poured into water, and extracted three times with methalene chloride. The extract was dried with sodium sulfate and concentrated to obtain 2.1 g of a black oil. The crude was purified by using two flash columns. The first was eluted with 1:1 hexanes:ether and the second with 20:1 methylene chloride:methanol. 130 mg of the title compound were collected as product. Following crystallization in ethanol and water, 66 mg of solid were recovered, m.p. 82° C. Analysis: Theory (.1/3 H2O): C, 82.37; H, 8.48; N, 7.68; Found: C, 82.33; H, 8.44; N, 7.73.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05426226
출처 데이터셋uspto-grants-1995_06
ORD IDord-e52d946ba6b940f2adfefdb638da511e
출처 메모uspto-grants-1995_06