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HRID 232310作成日:2026年10月27日

Hydrochloric Acid → alpha-(Bromomethyl)-4-(1H-imidazol-1-yl)benzenemethanol

https://huagongshe.com/reaction/232310

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)-HCID 11037—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物2-Bromo-1-[4-(1H-imidazol-1-yl)phenyl]ethanone hydrobromideHCID 20031310—
溶媒MethanolHCID 887—
生成物alpha-(Bromomethyl)-4-(1H-imidazol-1-yl)benzenemethanolHCID 20031362—

反応手順

Stir a mixture of 2-bromo-1-[4-(1H-imidazol-1-yl)-phenyl]ethanone hydrobromide (15.45 g, 44.6 mmol) and sodium cyanoborohydride (5.61 g, 89.3 mmol) in methanol (250 mL). Add a crystal of methyl orange and adjust the pH to 3.0 with 1.35M hydrochloric acid in methanol. Maintain the pH at 3.0 for about 2 hr. Treat the resulting solution with decolorizing carbon and filter through celite. Concentrate the filtrate and add water (200 mL) and methylene chloride (100 mL) to the residue. Adjust the pH to 7.5 with 2N NaOH solution. Separate the layers and extract the aqueous layer with methylene chloride (100 mL) and combine, dry over Na2SO4, filter and concentrate in vacuo. Add ethyl acetate to the residue to afford crystals of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04851526
出典データセットuspto-grants-1989_07
ORD IDord-4f7dcaa715774f9f894b866d61c454e1
出典メモuspto-grants-1989_07