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HRID 1368539作成日:2026年10月24日

Ammonium Chloride → (6-ethoxynaphthalen-2-yl)(1-trityl-1H-imidazol-4-yl)methanol

https://huagongshe.com/ja/reaction/1368539

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物2-Bromo-6-ethoxynaphthaleneHCID 236858—
反応物1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
反応物MagnesiumHCID 5462224—
触媒Methyl iodideHCID 6328—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(6-ethoxynaphthalen-2-yl)(1-trityl-1H-imidazol-4-yl)methanolHCID 2266497559.6%

反応手順

2-Bromo-6-ethoxynaphthalene (5.3 g) was dissolved in THF (40 ml). To the solution were added magnesium (0.515 g) and methyl iodide (one drop), and the mixture was vigorously stirred to dissolve magnesium. The reaction mixture was cooled in ice bath, and a solution of 4-formyl-1-tritylimidazole (7 g) in THF (80 ml) was added dropwise over 30 min, and the mixture was stirred at room temperature for 1 h. To the reaction mixture were added saturated aqueous solution of ammonium chloride (40 ml) and water (40 ml), and the mixture was extracted with ethyl acetate. The extract was washed with saturated sodium chloride solution, dried over magnesium sulfate and concentrated. The residue was washed with ethyl acetate to give (6-ethoxynaphthalen-2-yl)(1-trityl-1H-imidazol-4-yl)methanol (6.3 g) as a colorless powder. The product (6.3 g) was dissolved in dichloromethane (120 ml). To the solution was added manganese dioxide (6 g), and the mixture was stirred at room temperature over night. The reaction mixture was filtered with celite, and the filtrate was concentrated. The residue was crystallized from THF-ethyl acetate to give the titled compound (5.5 g) as a colorless powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06573289B1
出典データセットuspto-grants-2003_06
ORD IDord-6b0eb481b39a4ca887c42308485e4fbe
出典メモuspto-grants-2003_06