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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582969Generated: October 30, 2026

1,3-Dibromopropane → 5-Octyl-2-[4-(3-(2-(2-(pentafluoroethoxy) tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidine

https://huagongshe.com/reaction/582969

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-Hydroxyphenyl)-5-octylpyrimidineHCID 604055—
Reactant3-(2-(2-(Pentafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propyl bromideHCID 21225307—
SolventAcetonitrileHCID 6342—
Product5-Octyl-2-[4-(3-(2-(2-(pentafluoroethoxy) tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidineHCID 21225306—

Reaction Steps

The title compound was prepared essentially as in Example 1 by combining 5-octyl-2-(4-hydroxyphenyl)pyrimidine (2.0 g, 7.3 mmol), 3-(2-(2-(pentafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)-1-bromopropane (3.38 g, 7.47 mmol; prepared by combining 1,3-dibromopropane with 3-(2-(2-(pentafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethanol), and potassium carbonate (1.16 g, 8.43 mmol) in acetonitrile (20 mL) and refluxing the resulting mixture under nitrogen overnight. The mixture was cooled and filtered, and the resulting solids were washed with toluene (50 mL). The toluene was then removed under reduced pressure, and the resulting waxy solid was dissolved in toluene (50 mL) and washed with three 30 mL aliquots of perfluorohexane. After removing the toluene under reduced pressure, the resulting crude product was further purified by silica gel chromatography, eluting with 20 volume percent ethyl acetate/hexane, to yield 3.60 g of purified product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05928562
Source datasetuspto-grants-1999_07
ORD IDord-c96fc6514a1d4f8b8be00cebdb514ad7
Source noteuspto-grants-1999_07