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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 392582생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/392582

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물2-Bromo-6-ethoxynaphthaleneHCID 236858—
반응물1-(triphenylmethyl)-1H-imidazole-4-carbaldehydeHCID 618233—
반응물MagnesiumHCID 5462224—
촉매Methyl iodideHCID 6328—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(6-ethoxynaphthalen-2-yl)(1-trityl-1H-imidazol-4-yl)methanolHCID 2266497559.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06800778B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-bbb43dea9230438392dc61435eab668f
출처 메모uspto-grants-2004_10