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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1368539생성일: 2026년 10월 24일

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

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

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). 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06573289B1
출처 데이터셋uspto-grants-2003_06
ORD IDord-6b0eb481b39a4ca887c42308485e4fbe
출처 메모uspto-grants-2003_06