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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395200Generated: November 3, 2026

Hydrochloric Acid → HCID 22465771, compound

https://huagongshe.com/reaction/2395200

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—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 22465771HCID 2246577127.2%

Reaction Steps

In a Schlenk tube whose content had been replaced with Ar, 9.0 g of 60% sodium hydride and 400 ml of dry dimethoxyethane were placed. While this solution was being cooled with ice water, 29.8 g of 4,4'-dihydroxybiphenyl was added. Thereafter, the reaction solution was allowed to warm up to room temperature, and was stirred for two hours. Thereafter, the reaction solution was cooled to -60° C. After 86 g of 2-(perfluorobutyl)ethyl trifluoromethane sulfonate was added dropwise to the reaction solution, the reaction solution was allowed to warm up to room temperature, and was stirred overnight. Subsequently, the reaction solution was poured into dilute hydrochloric acid, and an organic layer was extracted with benzene. After the benzene layer was washed with water and dried over sodium sulfate anhydrous, the solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: benzene), and recrystallized from toluene to give 18.8 g of 4-hydroxy-4'-[2-(perfluorobutyl)ethyloxy]biphenyl (Y: 27.1%). The purity of the compound thus obtained was 98.4% by GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05814378
Source datasetuspto-grants-1998_09
ORD IDord-8b3315d4a87446fd969bc44c18c1a6f5
Source noteuspto-grants-1998_09