Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582996Generated: October 30, 2026

3-(2-(2-(2-(Trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propyl chloride → 2-Octyloxy-7-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)fluorene

https://huagongshe.com/reaction/582996

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-(2-(2-(Trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propyl chlorideHCID 21225290—
Reactant3-(2-(2-(2-(Trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propyl bromideHCID 21225395—
Reactant2-Octyloxy-7-hydroxyfluoreneHCID 21832462—
Product2-Octyloxy-7-(3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propoxy)fluoreneHCID 21225388—

Reaction Steps

The title compound was prepared essentially as in Example 1 by combining 2-octyloxy-7-hydroxyfluorene (1.0 g, 3.2 mmol) with a mixture of 3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propyl chloride and 3-(2-(2-(2-(trifluoromethoxy)tetrafluoroethoxy)tetrafluoroethoxy)-2,2-difluoroethoxy)propyl bromide (total 1.62 g, 3.3 mmol, 80:20 mole ratio). The reaction mixture was quenched by addition of water, and the resulting crude product was recrystallized from ethanol and further purified by Kugelrohr distillation (188° C. at 0.01 torr) to provide a yield of 0.84 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05928562
Source datasetuspto-grants-1999_07
ORD IDord-40f70ba16887488aaec23fbd3dbdc9e5
Source noteuspto-grants-1999_07