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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160212Generated: October 27, 2026

Sodium Azide → 2-Azido-1-(3-bromophenyl)ethan-1-ol

https://huagongshe.com/reaction/1160212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant[2-Bromo-1-(3-bromo-phenyl)-ethoxy]-trimethyl-silaneHCID 59515460—
SolventDimethyl SulfoxideHCID 679—
Product2-Azido-1-(3-bromophenyl)ethan-1-olHCID 57487857—

Reaction Conditions

Temperature80 °C

Reaction Steps

[2-Bromo-1-(3-bromo-phenyl)-ethoxy]-trimethyl-silane (5.85 g, 16.6 mmol and tetrabutyl sodium iodide (613 mg, 1.66 mmol) were dissolved in DMSO and sodium azide (2.16 g, 33.2 mmol) was slowly added. The mixture stirred at 80° C. for 4 hours and then at room temperature for 18 hours. The mixture was quenched with saturated sodium bicarbonate and extracted with ethyl acetate. The organics were washed with water brine and 1M HCl, then again with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography on silica gel, eluting with 5-10% ethyl acetate in hexanes. The title compound was isolated as a yellow oil (3.38 g, 83%). 1H NMR (300 MHz, CDCl3): 7.57 (s, 1H), 7.48 (d, 1H), 7.31-7.29 (m, 2H), 4.87 (m, 1H), 3.49 (d, 2H), 2.45 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816354B2
Source datasetuspto-grants-2010_10
ORD IDord-a765f5e5f31043ddb60440427b903fe1
Source noteuspto-grants-2010_10