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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183417Generated: November 3, 2026

Imidazole → 2-Bromo-6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]naphthalene

https://huagongshe.com/reaction/2183417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactant6-Bromo-2-naphthalenolHCID 27144—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDimethylformamideHCID 6228—
Product2-Bromo-6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]naphthaleneHCID 1347308364%

Reaction Steps

2-Bromo-6-hydroxynaphthalene (100.0 g, 0.45 mol) and imidazole (75.0 g, 1.10 mol) were dissolved in 300 mL of DMF. To this solution was added TBDMS-Cl (80.0 g, 0.53 mol). The reaction was stirred at room temperature under nitrogen overnight. The reaction was poured into water, and the precipitate was filtered, washed with water and cold ethanol. The crude product was recrystallized from ethanol to give 97.2 g of off-white crystals (64% yield). 1H NMR (CDCl3) δ ppm: 0.24 (s, 6 H), 1.01 (s, 9 H), 7.07 (dd, J1=8.8 Hz, J2=2.3 Hz, 1 H), 7.14 (s, 1 H), 7.45 (dd, J1=8.8 Hz, J2=2.3 Hz, 1 H), 7.53 (d, J=8.8 Hz, 1 H), 7.60 (d, J=8.8 Hz, 1 H), 7.90 (s, 1 H). 13C NMR (CDCl3) δ ppm: −4.34, 18.24, 25,68, 114.86, 117.26, 123.05, 128.29, 128.42, 129.39, 129.57, 130.24, 133.04. Mp 62-64° C. FD-MS: 337 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06899963B1
Source datasetuspto-grants-2005_05
ORD IDord-ef79f7b0158c4b498bc9a3528612c6b1
Source noteuspto-grants-2005_05