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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(4-Hydroxyphenyl)-5-octylpyrimidine | HCID 604055 | — |
| Reactant | 3-(2-(2-(Pentafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propyl bromide | HCID 21225307 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Octyl-2-[4-(3-(2-(2-(pentafluoroethoxy) tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05928562 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-c96fc6514a1d4f8b8be00cebdb514ad7 |
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| Source note | uspto-grants-1999_07 |
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