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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 727967Erstellt: 25. Oktober 2026

1-Bromodecane → [1,1'-Biphenyl]-4-carbonitrile, 4'-(decyloxy)-

https://huagongshe.com/reaction/727967

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BromodecaneHCID 8173—
EduktPotassium CarbonateHCID 11430—
Edukt4'-Hydroxy-4-biphenylcarbonitrileHCID 140610—
LösungsmittelMethyl Isobutyl KetoneHCID 7909—
Produkt[1,1'-Biphenyl]-4-carbonitrile, 4'-(decyloxy)-HCID 11240597%

Reaktionsschritte

To 30 ml of methyl isobutyl ketone were added 3 g of 4-hydroxy-4'-cyanobiphenyl, 21.4 g of 1-bromodecane and 2.5 g of potassium carbonate, and the mixture was reacted under reflux for 30 hours. The reaction mixture was cooled and insoluble substances were removed by filtration. The filtrate was concentrated under a reduced pressure, ethanol was added to the residue and recrystallization was carried out to obtain 5 g of 4-decyloxy-4'-cyanobiphenyl. Thus, 4.1 g of this 4-decyloxy-4'-cyanobiphenyl was dissolved in 25 ml of ethylene glycol, 2.5 ml of 2N sodium hydroxide was added to the solution, and a reaction was carried out under reflux for 4 hours. The reaction liquid was put into dilute hydrochloric acid cooled by ice, and the precipitate was recovered by filtration, washed with water and ethanol, and dried. The dried product was recrystallized from chloroform to obtain 3.0 g of 4'-decyloxybiphenyl-4-carboxylic acid. Then, 20 g of thionyl chloride was dropped into this carboxylic acid and the mixture was reacted under reflux for 2 hours. Unreacted thionyl chloride was removed by distillation under a reduced pressure and 4'-decyloxybiphenyl-4-carboxylic acid chloride was quantitatively recovered.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05045228
Quelldatensatzuspto-grants-1991_09
ORD IDord-326b98ea0bee497fa1cfc96feb27b4d3
Quellennotizuspto-grants-1991_09