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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423452생성일: 2026년 10월 25일

4-Bromophenol → 4'-(Methylsulfonyl)-[1,1'-biphenyl]-4-ol

https://huagongshe.com/reaction/423452

반응식

참여 물질

역할이름HCID투입량
반응물4-BromophenolHCID 7808—
반응물Sodium CarbonateHCID 10340—
반응물4-(Methanesulfonyl)phenylboronic acidHCID 2734364—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
생성물4'-(Methylsulfonyl)-[1,1'-biphenyl]-4-olHCID 1498267664%

반응 조건

온도90 °C

반응 단계

[4-(Methylsulfonyl)phenyl]boronic acid (0.69 g, 3.40 mmol) was added to a solution of 4-bromophenol (0.5 g, 2.83 mmol) in DME (25 mL), followed by addition of 2M Na2CO3 (25 mL) and Pd(PPh3)4 (0.17 g, 0.14 mmol). The reaction mixture was heated at 90° C. for 3 h, then cooled to ambient temperature, and extracted with ether. The combined organic extract was washed with brine, dried over Na2SO4, filtered, and the filtrate was concentrated to give the crude product as an off-white solid. The crude product was purified by chromatography on a silica gel column eluted with 50% EtOAc/hexane to give 0.45 g (64%) of 4′-(methylsulfonyl)-4-biphenylol as a white solid. Alternatively, 4′-(methylsulfonyl)-4-biphenylol was prepared from 4-bromophenyl methyl sulfone (2 g, 8.5 mmol), (4-hydroxyphenyl)boronic acid (1.76 g, 12.75 mmol), 2M Na2CO3 (100 mL) and Pd(PPh3)4 (0.1 g, 0.08 mmol) in DME (100 mL) in a manner similar to the conditions above. 1H NMR (400 MHz, CDCl3): δ 7.97 (d, 2H, J=8.6 Hz), 7.71 (d, 2H, J=8.3 Hz), 7.51 (d, 2H, J=8.6 Hz), 6.94 (d, 2H, J=8.5 Hz), 4.92 (s, 1H), 3.08 (s, 3H); LRMS (ESI), m/z 249 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101634B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-cc1c6b97e4c744338c51e2fe36413402
출처 메모uspto-grants-2012_01