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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873321Generated: October 30, 2026

Ethyl Bromide → (3-Ethoxy-5,6-difluoronaphthalen-2-yl)trimethylsilane

https://huagongshe.com/reaction/1873321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
Reactant7,8-Difluoro-3-trimethylsilanylnaphthalen-2-olHCID 58151937—
SolventMethyl Ethyl KetoneHCID 6569—
Product(3-Ethoxy-5,6-difluoronaphthalen-2-yl)trimethylsilaneHCID 58151894—

Reaction Steps

54.7 g (about 0.12 mol) of 7,8-difluoro-3-trimethylsilanylnaphthalen-2-ol are stirred at 80° C. for 19 h together with 19.5 ml (0.26 mol) of bromoethane and 34.5 g (0.25 mol) of potassium carbonate in 400 ml of ethyl methyl ketone. The batch is filtered, and the residue is washed with ethyl methyl ketone. The filtrate is concentrated, and the residue is taken up in MTBE. The solution is washed with water and sat. sodium chloride soln. and dried using sodium sulfate. The residue remaining after removal of the solvent is purified by column chromatography (SiO2, toluene:ethyl acetate=9:1), giving (3-ethoxy-5,6-difluoronaphthalen-2-yl)trimethylsilane as a dark-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08303844B2
Source datasetuspto-grants-2012_11
ORD IDord-156dac9c313249acadc8205f37becccb
Source noteuspto-grants-2012_11