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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289378Generated: October 26, 2026

Hydrochloric Acid → 2,3-Difluoro-4'-[12,12-bis(ethoxycarbonyl)dodecyl]oxybiphenyl

https://huagongshe.com/reaction/1289378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium ethoxideHCID 2723922—
Reactant2,3-Difluoro-4'-(11-bromoundecyl)oxybiphenylHCID 18920856—
SolventTetrahydrofuranHCID 8028—
Product2,3-Difluoro-4'-[12,12-bis(ethoxycarbonyl)dodecyl]oxybiphenylHCID 1892083884.7%

Reaction Steps

First, 0.62 g of sodium ethoxide, 1.5 g of diethyl malonate, and 50 ml of dry ethanol were placed in a 100 ml flask whose content was replaced with argon. Then, 20 ml of tetrahydrofuran solution in which 4 g of 2,3-difluoro-4'-(11-bromoundecyl)oxybiphenyl was dissolved was added dropwise to the reaction mixture, and the resultant reaction mixture was stirred under reflux for 8 hours. The reaction mixture was poured into diluted hydrochloric acid, and an organic layer was extracted with ether. The ether layer was washed with water and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away. The residue was purified by silica gel column chromatography (eluent: toluene) to obtain 4 g of 2,3-difluoro-4'-[12,12-bis(ethoxycarbonyl)dodecyl]oxybiphenyl (Y: 84.7%). The compound thus obtained had a purity of 99.8% by GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750213
Source datasetuspto-grants-1998_05
ORD IDord-737b20e0ab864dca948446b5066447cd
Source noteuspto-grants-1998_05