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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1936327생성일: 2026년 10월 27일

Ethanol → HCID 178444293, 화합물

https://huagongshe.com/reaction/1936327

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물5-Bromo-1,3-difluoro-2-iodobenzeneHCID 2782702—
반응물HCID 178444242HCID 178444242—
촉매HCID 178418397HCID 178418397—
용매BenzeneHCID 241—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물HCID 178444293HCID 17844429339.1%

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06388146B1
출처 데이터셋uspto-grants-2002_05
ORD IDord-66da78fe7e7f4b39a300355dfbd4cd1d
출처 메모uspto-grants-2002_05