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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 735313생성일: 2026년 10월 24일

Ammonia → (1S)-1-(2-{[6-(2,4-Difluorophenyl)-2-naphthyl]sulfonyl}phenyl)ethanol

https://huagongshe.com/ko/reaction/735313

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참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물1-(2-Bromophenyl)ethan-1-olHCID 6950331—
반응물HCID 68899091HCID 68899091—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
생성물(1S)-1-(2-{[6-(2,4-Difluorophenyl)-2-naphthyl]sulfonyl}phenyl)ethanolHCID 6890113426.5%

반응 조건

온도110 °C

반응 단계

Sodium 6-(2,4-difluorophenyl)naphthalene-2-sulfinate (Step 3, 486 mg, 1.49 mmol), (1S)-1-(2-bromophenyl)ethanol (260 mg, 1.29 mmol) and copper(I) iodide (1.23 g, 6.46 mmol) were combined in dimethylsulfoxide (10 mL) and degassed. The reaction was heated to 110° C. for 2 hours. The cooled reaction mixture was poured into conc. ammonia solution and extracted with diethyl ether (x4). The combined organic layers were washed with brine, dried over MgSO4 and evaporated in vacuo. The residue was purified by flash column chromatography on silica, eluting with 5% then 10% diethyl ether/dichloromethane, followed by trituration with isohexane. A second column, eluting with 60% diethyl ether/isohexane, followed by trituration with isohexane, gave the title compound (145 mg). 1H NMR (500 MHz, CDCl3) δ 8.56 (1H, s), 8.17 (1H, d, J=7.9 Hz), 8.06-7.98 (3H, m), 7.79-7.76 (3H, m), 7.66 (1H, t, J=7.5 Hz), 7.54-7.48 (2H, m), 7.03-6.95 (2H, m), 5.65 (1H, q, J=6.2 Hz), 2.51 (1H, s), 1.35 (3H, d, J=6.3 Hz); m/z (ES+) 407 [(M-OH)+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07592456B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-e30a3a2243824c7abfb49235fe7dd579
출처 메모uspto-grants-2009_09