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HRID 12382作成日:2026年10月25日

2,4,6-Trimethylpyridine → 4,4-Dimethyl-1-(2-nitrophenyl)-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/12382

反応式

関与物質

役割名称HCID仕込み量
反応物2,4,6-TrimethylpyridineHCID 7953—
反応物1-Fluoro-2-nitrobenzeneHCID 73895—
反応物4,4-Dimethyl-1,2,3,4-tetrahydroquinolineHCID 13219441—
溶媒ChloroformHCID 6212—
生成物4,4-Dimethyl-1-(2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 57423310—

反応条件

温度250 °C

反応手順

1b (0.762 g, 4.73 mmol), ortho-fluoronitrobenzene (0.88 g, 5.67 mmol, 1.19 eq), and 2,4,6-collidine (0.66 mL, 1.05 eq) were pre-stirred 40s in a conical microwave container. It was then heated with stirring at a Personal Chemistry Microwave reactor with normal absorption at 250° C. for 1 h. The crude mixture was dissolved in CHCl3, and was purified by flash chromatography (hexanes/EtOAc) to give 0.66 g of crude 1c. LC-MS ESI 283 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728008B2
出典データセットuspto-grants-2010_06
ORD IDord-6f4b0b70237f463091d7218d522edefa
出典メモuspto-grants-2010_06