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HRID 392582作成日:2026年10月26日

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

https://huagongshe.com/reaction/392582

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) and magnesium (0.515 g) and methyl iodide (one drop) were added and the mixture was vigorously stirred to dissolve magnesium. The reaction mixture was ice-cooled and a solution of 4-formyl-1-tritylimidazole (7 g) in THF (80 ml) was added dropwise over 30 min. The mixture was stirred at room temperature for 1 h. To the reaction mixture were added saturated aqueous solution (40 ml) of ammonium chloride and water (40 ml) and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, 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. This product (6.3 g) was dissolved in dichloromethane (120 ml) and manganese dioxide (6 g) was added. The mixture was stirred at room temperature overnight. The reaction mixture was filtered through Celite and the filtrate was concentrated. The residue was crystallized from THF-ethyl acetate to give the title compound (5.5 g) as a colorless powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06800778B1
出典データセットuspto-grants-2004_10
ORD IDord-bbb43dea9230438392dc61435eab668f
出典メモuspto-grants-2004_10