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HRID 1825049作成日:2026年10月26日

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

https://huagongshe.com/reaction/1825049

反応式

関与物質

役割名称HCID仕込み量
反応物Aluminum isopropoxideHCID 11143—
反応物AzidotrimethylsilaneHCID 78378—
反応物2-(3-Bromophenyl)oxiraneHCID 147193—
反応物Potassium sodium tartarateHCID 9855836—
溶媒DichloromethaneHCID 6344—
生成物2-Azido-2-(3-bromophenyl)ethan-1-olHCID 2214503129%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07045551B2
出典データセットuspto-grants-2006_05
ORD IDord-1a34632c1a494f80923ef844923a5cde
出典メモuspto-grants-2006_05