戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 22139作成日:2026年10月26日

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

https://huagongshe.com/reaction/22139

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-ChloroquinolineHCID 11928—
反応物MagnesiumHCID 5462224—
反応物8-Bromo-2-dipropylamino-1,2,3,4-tetrahydronaphthaleneHCID 14529564—
触媒1,2-DibromoethaneHCID 7839—
溶媒TetrahydrofuranHCID 8028—
生成物2-Di-n-propylamino-8-(quinol-2-yl)-1,2,3,4-tetrahydronaphthaleneHCID 23373524181.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426226
出典データセットuspto-grants-1995_06
ORD IDord-e52d946ba6b940f2adfefdb638da511e
出典メモuspto-grants-1995_06