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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1936327Erstellt: 26. Oktober 2026

Ethanol → HCID 178444293, Verbindung

https://huagongshe.com/reaction/1936327

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
Edukt5-Bromo-1,3-difluoro-2-iodobenzeneHCID 2782702—
EduktHCID 178444242HCID 178444242—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktHCID 178444293HCID 17844429339,1%

Reaktionsschritte

First, 50 ml of ethanol containing 5.61 g of 4-(trans-4-pentylcyclohexyl)phenylboronic acid dissolved therein, 50 ml of benzene containing 5.0 g of 4-bromo-2,6-difluoro-1-iodobenzene dissolved therein, 15.7 ml of a sodium carbonate aqueous solution with a concentration of 2.0 mol/l, and 0.45 g of tetrakis(triphenylphosphine)palladium(0) were put in an argon-replaced 200 ml flask, and stirred under reflux for 48 hours. After the reaction, water and ether were added to the reaction solution for extraction. The resultant ether 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:hexane) and recrystallized from acetone, to obtain 2.58 g (Y: 39.1%) of 4-bromo-2,6-difluoro-4′-(trans-4-pentylcyclohexyl)biphenyl. The purity of the resultant compound was 100.0% as measured by GC. (5-b) Synthesis of polymerizable compound 2,6-difluoro-4′-(trans-4-pentylcyclohexyl)-4-vinylbiphenyl represented by formula (E) above

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06388146B1
Quelldatensatzuspto-grants-2002_05
ORD IDord-66da78fe7e7f4b39a300355dfbd4cd1d
Quellennotizuspto-grants-2002_05