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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1816596생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1816596

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 tetrahydrofuran and 100 ml ethanol. 1 g of sodium borohydride was added thereto, followed by stirring overnight at room temperature. After adding 1 N hydrochloric acid thereto, the reaction solution was extracted with ethyl acetate, and the organic layer was washed with water and brine, 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 N,N-dimethylformamide, and 1.8 g of imidazole and 5.9 g of tertiary butyl chlorodiphenyl silane were added, and the mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with water and brine, dried over anhydrous magnesium sulfate and the solvent was evpoarated, to give 10.72 g of [(5-bromo-2,3-dimethoxybenzyl)oxy](tertiary butyl)diphenylsilane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06884821B1
출처 데이터셋uspto-grants-2005_04
ORD IDord-2a715fa163dd400bbad657b9fe6ea544
출처 메모uspto-grants-2005_04