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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232310생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/232310

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)-HCID 11037—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물2-Bromo-1-[4-(1H-imidazol-1-yl)phenyl]ethanone hydrobromideHCID 20031310—
용매MethanolHCID 887—
생성물alpha-(Bromomethyl)-4-(1H-imidazol-1-yl)benzenemethanolHCID 20031362—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04851526
출처 데이터셋uspto-grants-1989_07
ORD IDord-4f7dcaa715774f9f894b866d61c454e1
출처 메모uspto-grants-1989_07