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HRID 516797생성일: 2026년 10월 25일

Ammonium Chloride → Tris(2,4-dimethoxyphenyl)methanol

https://huagongshe.com/reaction/516797

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물1-Bromo-2,4-dimethoxybenzeneHCID 87266—
반응물Benzoic acid, 2,4-dimethoxy-, methyl esterHCID 137451—
용매Diethyl EtherHCID 3283—
생성물Tris(2,4-dimethoxyphenyl)methanolHCID 44630337—

반응 단계

Add (4.23 g, 19.47 mmol) 1-bromo-2,4-dimethoxybenzene to an appropriately sized round bottom flask. Attach a rubber septum to seal the flask. Insert a needle into the septum as a vent and flush the round bottom flask with nitrogen for about 10 minutes. Add anhydrous ether (80 mL), followed by the drop wise addition of n-butyllithium in hexane (1.6M, 12.2 mL). Stir the cloudy mixture for 10 minutes and keep the round bottom flask on ice. Dissolve (2.20 g, 9.74 mmol) of methyl 2,4-dimethoxybenzoate in about 20 ml of anhydrous ether (if needed, more than about 20 ml can be used), and then add this drop wise to the reaction mixture. After the addition is complete, stir the reaction mixture for about 3 minutes longer. Pour the reaction mixture into a separatory funnel containing 5% NH4Cl (aq) (50 mL) and shake until a color change is observed (pale orange). The layers are allowed to separated, and dry the top ether layer with about 5 g anhydrous Na2SO4, filter, and the volatiles were removed in a rotary evaporator to dryness at 35-40° C. under 400 mbar. Place the crude oil of hexamethoxy red (yellow-orange in color) into the freezer. Yield is about 3.1 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115066B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-46f242c095aa45f9b22bb4b4a66bf3c2
출처 메모uspto-grants-2015_08