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HRID 277841생성일: 2026년 10월 25일

Sodium Carbonate → 4-Amino-3'-chloro-biphenyl-3-carbonitrile

https://huagongshe.com/reaction/277841

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참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-Amino-5-bromobenzonitrileHCID 429740—
반응물(3-Chlorophenyl)boronic acidHCID 2734323—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물4-Amino-3'-chloro-biphenyl-3-carbonitrileHCID 979457587%

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온도85 °C

반응 단계

A mixture of 2-amino-5-bromobenzonitrile (10 g, 50 mmol), 3-chlorophenyl boronic acid (9.5 g, 60 mmol), tetrakis(triphenylphosphine)-palladium(0) (3.5 g, 3 mmol), and sodium carbonate (13 g, 120 mmol) in a mixture of DME and water (100 mL/25 mL) was degassed to remove the oxygen and then heated to 85° C. under a blanket of nitrogen for 5 hours. The reaction mixture was cooled to ambient temperature and quenched with a saturated aqueous ammonium chloride solution (80 mL). Ethyl acetate (200 mL) was added, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate (3×40 mL). The combined organic layers were washed with brine and dried with MgSO4. The solvent was removed in vacuo and the residue was purified by a silica gel flash chromatography (hexane:ethyl acetate/4:1) to afford 4-amino-3′-chloro-biphenyl-3-carbonitrile as an off-white solid (8 g, 87%): mp 118-119° C.; 1H-NMR (DMSO-d6) δ 7.80 (d, 1H, J=2.3 Hz), 7.65-7.72 (m, 2H), 7.57 (d, 1H, J=8.0 Hz), 7.42 (t, 1H, J=7.9 Hz), 7.31 (m, 1H), 6.87 (d, 1H, J=8.7 Hz), 6.29 (br, 2H); Anal. Calc. For C13H9ClN2: C, 68.28, H. 3.97, N, 12.25. Found: C, 67.68, H, 4.06, N, 11.89.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06358948B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-fa0e369105694122b8b550d0d3fac306
출처 메모uspto-grants-2002_03