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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257477Generated: October 30, 2026

5-Octyl-2-[4-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidine → 5-Heptyloxy-2-[4-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidine

https://huagongshe.com/reaction/2257477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Octyl-2-[4-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidineHCID 21225304—
Reactant5-Heptyloxy-2-(4-hydroxyphenyl)pyrimidineHCID 135708812—
SolventDimethylformamideHCID 6228—
Product5-Heptyloxy-2-[4-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)phenyl]pyrimidineHCID 21225389—

Reaction Conditions

Temperature120 °C

Reaction Steps

The title compound was prepared essentially as in Example I by combining 3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy) 1-chloropropane (5.5 g, 15.0 mmol, Example 24) with 5-heptyloxy-2-(4-hydroxyphenyl)pyrimidine (3 g, 10.5 mmol) in dimethylformamide and stirring at 120° C. overnight to provide product boiling at 195°-210° C. at 0.3 torr (yield of 5.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658491
Source datasetuspto-grants-1997_08
ORD IDord-0a2f4a19d6c94f6394d22e8408e133d7
Source noteuspto-grants-1997_08