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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1296204생성일: 2026년 10월 27일

Hydrochloric Acid → (5-Bromo-2,3-dimethoxyphenyl)methanol

https://huagongshe.com/reaction/1296204

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물5-Bromo-2,3-dimethoxybenzaldehydeHCID 322405—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물(5-Bromo-2,3-dimethoxyphenyl)methanolHCID 219409095.5%

반응 단계

10.67 g of 5-bromo-2,3-dimethoxybenzaldehyde was dissolved in 100 ml of tetrahydrofuran and 100 ml of ethanol, and 1 g of sodium borohydride was added, and then the solution was stirred overnight at room temperature. 1 N hydrochloric acid was added thereto, followed by extracting with ethyl acetate. The organic layer was washed with water and an aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate and the solvent was evaporated, to give 10.27 g of 5-bromo-2,3-dimethoxybenzyl alcohol. 5.326 g of this crude product was dissolved in 50 ml of N,N-dimethylformamide, and 1.8 g of imidazole and 5.9 g of t-butylchlorodiphenylsilane were added thereto, and the solution was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and the solvent was evaporated, to give 10.72 g of [(5-bromo-2,3-dimethoxybenzyl)oxy](t-butyl)diphenylsilane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07244861B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-7f4299c661c64149a844fba7d3690b01
출처 메모uspto-grants-2007_07