Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582974Generated: October 30, 2026

2-(4-Hydroxyphenyl)-5-octylpyrimidine → 5-Octyl-2-[4-(4-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)butoxy)phenyl]pyrimidine

https://huagongshe.com/reaction/582974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Hydroxyphenyl)-5-octylpyrimidineHCID 604055—
Reactant4-(2-(2-(2-(Trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy) 1-bromobutaneHCID 21225287—
Product5-Octyl-2-[4-(4-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)butoxy)phenyl]pyrimidineHCID 21225381—

Reaction Steps

The title compound was prepared essentially as in Example 1 by combining 4-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)-1-bromobutane (20.9 g, 38.5 mol; prepared from 1,4-dibromobutane and 2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethanol) with 5-octyl-2-(4-hydroxyphenyl)pyrimidine (10.0 g, 0.35 mol). The resulting product was further purified by recrystallization from ethanol and subsequent Kugelrohr distillation to provide a yield of 17.5 g (b.p. 195-220° C. at 0.1 torr).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05928562
Source datasetuspto-grants-1999_07
ORD IDord-d29aff48d0f84754acf59f3bb858b2ae
Source noteuspto-grants-1999_07