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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413620생성일: 2026년 10월 23일

Trisodium phosphate dodecahydrate → 4'-n-Propyl-3,5-difluoro-biphenyl-4-ylamine

https://huagongshe.com/ko/reaction/413620

반응식

참여 물질

역할이름HCID투입량
반응물Trisodium phosphate dodecahydrateHCID 61473—
반응물4-Bromo-2,6-difluoroanilineHCID 610191—
반응물(4-Propylphenyl)boronic acidHCID 4100861—
촉매Bis(triphenylphosphine)palladiumHCID 10122028—
용매WaterHCID 962—
생성물4'-n-Propyl-3,5-difluoro-biphenyl-4-ylamineHCID 7000995699.5%

반응 단계

348 g trisodiumphosphate dodecahydrate (Merck KGaA, Art. No.106 578) were dissolved in 500 ml of distilled water. Then 8.563 g bis(triphenylphosphine) palladium (Merck KGaA, Art. No. 804 174) and 0.611 g hydaziniumhydroxide (Merck KGaA, Art. No. 804 604) were added. The suspension was stirred for 5 minutes. Then, 126.886 g 4-bromo-2,6-difluoro-aniline, prepared in house, were added. Next 100 g of the p-n-propylphenyl boronic acid, prepared as described above, dissolved in 600 ml dried tetrahydrafurane (Merck KGaA, Art. No.108 107) was added dropwise. The reaction mixture was heated 6 hours under reflux. The organic layer was separated, dried over Na2SO4 and it's solvent evaporated. The isolated crude product (150 g of 4′-n-propyl-3,5-difluoro-biphenyl-4-ylamine was used for the next step of the reaction without further purificatoin.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06569505B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-4abd16b979e747879e943d62a7d5e4d7
출처 메모uspto-grants-2003_05