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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358810Generated: October 31, 2026

1-Bromohexane → HCID 14745781, compound

https://huagongshe.com/reaction/358810

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexaneHCID 8101—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium tertbutoxideHCID 50987170—
ReactantHCID 135736655HCID 135736655—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 14745781HCID 1474578174%

Reaction Steps

0.5 g of 2-(3-fluoro-4-hydroxyphenyl)-5-(4-heptylphenyl)pyrimidine and 0.185 g of potassium-tertbutoxide were dissolved in 20 ml of dimethyl sulfoxide. The resulting solution was stirred at room temperature for 30 minutes and then 0.295 of n-hexyl bromide was added dropwise thereto. After the completion of the addition, the mixture was stirred at room temperature for six hours. Then 100 ml of ethyl acetate and 100 ml of water were added to the reaction mixture and the organic layer was repeatedly washed with water until the pH value of the aqueous layer became neutral. Subsequently the organic layer was separated and dried over anhydrous sodium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (developing solvent: toluene) and then recrystallized from ethanol. Thus 0.467 g of 2-(3-fluoro-4-hexyloxyphenyl)-5-(4-heptylphenyl)pyrimidine was obtained. Yield: 74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997942
Source datasetuspto-grants-1991_03
ORD IDord-aa0538b45f0243d4a972d5de8f2bbe54
Source noteuspto-grants-1991_03