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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1825049생성일: 2026년 10월 25일

Aluminum isopropoxide → 2-Azido-2-(3-bromophenyl)ethan-1-ol

https://huagongshe.com/reaction/1825049

반응식

참여 물질

역할이름HCID투입량
반응물Aluminum isopropoxideHCID 11143—
반응물AzidotrimethylsilaneHCID 78378—
반응물2-(3-Bromophenyl)oxiraneHCID 147193—
반응물Potassium sodium tartarateHCID 9855836—
용매DichloromethaneHCID 6344—
생성물2-Azido-2-(3-bromophenyl)ethan-1-olHCID 2214503129%

반응 단계

To a solution of 2-(3-bromo-phenyl)-oxirane (2.5 g, 12.6 mmol) in CH2Cl2 (20 mL) was added azidotrimethylsilane (2.5 mL, 18.84 mmol), followed by aluminium isopropoxide (256 mg, 1.26 mmol). The reaction mixture was stirred at room temperature for 18 h. Sodium potassium tartrate 1M (30 mL) was added, the aqueous layer was extracted with CH2Cl2, and the organic layers were dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo, and the crude compound is purified by flash chromatography (10% EtOAc/Hex) to provide 2-azido-2-(3-bromo-phenyl)-ethanol (876 mg, 29%). To a solution of 2-azido-2-(3-bromo-phenyl)-ethanol (876 mg) in THF (10 mL) was added polymer supported triphenylphosphine (3 mmol/g) (2 g, 6 mmol), and the mixture was heated to 60° C. for 30 min. The polymer was then filtered and washed with CH2Cl2. The polymer was suspended in THF (20 mL) and concentrated NH4OH (10 mL) was added, and this mixture was agitated for 24 h. The polymer was filtered and the liquid phase was evaporated in vacuo to afford the title compound (110 mg, 14%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07045551B2
출처 데이터셋uspto-grants-2006_05
ORD IDord-1a34632c1a494f80923ef844923a5cde
출처 메모uspto-grants-2006_05