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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253554생성일: 2026년 10월 26일

2-Bromophenol → 1-Bromo-2-(2-ethylphenoxy)benzene

https://huagongshe.com/reaction/253554

반응식

참여 물질

역할이름HCID투입량
반응물2-BromophenolHCID 7244—
반응물TriethylamineHCID 8471—
반응물2-Ethylphenylboronic Acid (contains varying amounts of Anhydride)HCID 4100862—
촉매Cupric acetateHCID 8895—
용매DichloromethaneHCID 6344—
생성물1-Bromo-2-(2-ethylphenoxy)benzeneHCID 5741961331%

반응 단계

To a solution of 2-ethylphenylboronic acid (4.50 g, 30 mmol), 2-bromophenol (3.54 g, 20 mmol), and Cu(OAc)2 (1.86 g, 10 mmol) in anhydrous CH2Cl2 (50 mL) were added activated 4 Å molecular sieves (˜0.5 g), followed by anhydrous Et3N (7.0 mL, 50 mmol). The resulting dark green solution was stirred at rt for 48 h. The solvent was removed under vacuum and the residue was triturated several times with ether (˜200 mL). The combined organic solutions were washed with satd aq NH4Cl, and 1 N aq HCl aqueous solution, and solvent was removed under vacuum to give a crude product. Flash column chromatography gave 1-bromo-2-(2-ethylphenoxy)benzene (1.72 g, 31%) as a clear oil; 1H NMR (CDCl3, 400 MHz) δ: 7.62 (dd, 1H), 7.28 (m, 1H), 7.22-7.08 (m, 3H), 6.96 (m, 1H), 6.78 (m, 2H), 2.64 (q, 2H), 1.22 (t, 3H); MS no ionization was observed.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872028B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-43699f6428104e0ebb0068ca970a8f32
출처 메모uspto-grants-2011_01