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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653814Generated: November 1, 2026

1-Bromononane → 2-(3-Fluoro-4-n-nonyloxyphenyl)-5-(4-n-hexylphenyl)pyrazine

https://huagongshe.com/reaction/653814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromononaneHCID 12742—
ReactantPotassium tertbutoxideHCID 50987170—
Reactant2-(3-Fluoro-4-hydroxyphenyl)-5(4-n-hexylphenyl)pyrazineHCID 135736654—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-(3-Fluoro-4-n-nonyloxyphenyl)-5-(4-n-hexylphenyl)pyrazineHCID 1471610086.1%

Reaction Steps

0.35 g of the crude 2-(3-fluoro-4-hydroxyphenyl)-5(4-n-hexylphenyl)pyrazine was dissolved in 3 ml of dimethyl sulfoxide and 3 ml of tetrahydrofuran. To the resulting solution, was added 0.12 g of potassium-tertbutoxide. The obtained mixture was stirred at room temperature for 30 minutes and then 0.22 g of n-nonyl bromide was added thereto. The mixture was stirred at room temperature for additional five hours. Then the reaction mixture was diluted with ethyl acetate, washed with dilute hydrochloric acid and with a 30% aqueous solution of sodium hydroxide and the repeatedly washed with water until the washing liquor showed a pH value of approximately 7. Then the ethyl acetate phase was dehydrated over sodium sulfate and the solvent was distilled off. Thus 0.48 g of a crude reaction product was obtained. The crude reaction product was purified by silica gel column chromatography and recrystallized from acetone. Thus 0.41 g of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05128472
Source datasetuspto-grants-1992_07
ORD IDord-ee887bad155c46c1bb5c616323361bf0
Source noteuspto-grants-1992_07