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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936337Generated: October 31, 2026

Hydrochloric Acid → HCID 22465771, compound

https://huagongshe.com/reaction/1936337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4,4'-DihydroxybiphenylHCID 7112—
ReactantSodium hydrideHCID 24758—
Reactant3,3,4,4,5,5,6,6,6-Nonafluorohexyl trifluoromethanesulfonateHCID 22465757—
SolventBenzeneHCID 241—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 22465771HCID 2246577127.2%

Reaction Steps

First, 3.0 g of 60% sodium hydride and 120 ml of dehydrated dimethoxyethane were put in an argon-replaced 300 ml flask. Then, 9.93 g of 4,4′-dihydroxybiphenyl was added while icing, and stirred at room temperature for two hours. The reaction solution was cooled again to −60° C., and 28.7 g of 2-(perfluorobutyl)ethyl trifluoromethanesulfonate was dropped into the reaction solution. After the resultant reaction solution was left to resume room temperature, it was stirred for 12 hours. After the reaction, dilute hydrochloric acid and benzene were added to the reaction solution to separate an organic layer. The organic layer was washed with a saturated brine and dried with sodium sulfate. The solvent was then distilled off. The residue was purified by silica gel column chromatography (eluent:benzene/ethyl acetate=9/1), and recrystallized from toluene to obtain 6.26 g (Y: 27.1%) of 4-hydroxy-4′-[2-(perfluorobutyl)ethyloxy]biphenyl. The purity of the resultant compound was 98.4% as measured by GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06388146B1
Source datasetuspto-grants-2002_05
ORD IDord-cd04289144b74407a9a4b1c61334cdc3
Source noteuspto-grants-2002_05