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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727967생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/727967

반응식

참여 물질

역할이름HCID투입량
반응물1-BromodecaneHCID 8173—
반응물Potassium CarbonateHCID 11430—
반응물4'-Hydroxy-4-biphenylcarbonitrileHCID 140610—
용매Methyl Isobutyl KetoneHCID 7909—
생성물[1,1'-Biphenyl]-4-carbonitrile, 4'-(decyloxy)-HCID 11240597%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05045228
출처 데이터셋uspto-grants-1991_09
ORD IDord-326b98ea0bee497fa1cfc96feb27b4d3
출처 메모uspto-grants-1991_09