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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 560114생성일: 2026년 10월 27일

3-Bromobenzaldehyde → 2-Amino-1-(3-bromophenyl)ethan-1-ol

https://huagongshe.com/reaction/560114

반응식

참여 물질

역할이름HCID투입량
반응물3-BromobenzaldehydeHCID 76583—
반응물DiisopropylethylamineHCID 81531—
반응물Trimethylsilyl cyanideHCID 82115—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물2-Amino-1-(3-bromophenyl)ethan-1-olHCID 22021067—

반응 단계

To a cooled solution of 3-bromobenzaldehyde (1.58 mL) in THF (15 mL) were added trimethylsilyl cyanide (1.7 mL) and N,N-diisopropylethylamine (0.23 mL). The mixture was stirred at room temperature for 2d and at reflux for 2 h. The solution was allowed to cool to room temperature and then was slowly added to a cooled suspension of lithium aluminium hydride (769 mg) in THF (10 mL). The mixture was stirred at 0° C. for 10 min, the cooling bath was removed, and the mixture was heated at reflux for 3 h. After cooling to room temperature, ethylacetate was added slowly, followed by a mixture of Na2SO4/silicagel/H2O. After stirring the suspension for 30 min, the mixture was filtered, the filtrate was dried (Na2SO4), and concentrated in vacuo. The residue was purified by chromatography (SiO2, CH2Cl2/MeOH/ammonia 90:10:2) to give (1.59 g) 2-amino-1-(3-bromo-phenyl)-ethanol as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063088B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-92924f80a4c84f7787d895da1891166a
출처 메모uspto-grants-2011_11