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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432221생성일: 2026년 10월 24일

3-Phenoxybenzyl alcohol → (2-Bromo-5-phenoxyphenyl)methanol

https://huagongshe.com/ko/reaction/432221

반응식

참여 물질

역할이름HCID투입량
반응물3-Phenoxybenzyl alcoholHCID 26295—
반응물N-bromobutanimideHCID 67184—
용매AcetonitrileHCID 6342—
생성물(2-Bromo-5-phenoxyphenyl)methanolHCID 2234675885%

반응 단계

To a solution of 3-phenoxyphenyl methanol (4.0 g, 0.020 mol) in anhydrous acetonitrile was added 1-bromo-2,5-pyrrolidinedione (3.73 g, 0.021 mol) at room temperature. The mixture was stirred at room temperature for one and a half hour under an atmosphere of nitrogen. The solvents were removed under the reduced pressure. Tetrachloromethane (100 mL) was added to the residue, and the mixture was filtered. The filtrate was concentrated into the residue, and the residue was purified by flash chromatography on silica gel using ethyl acetate/n-heptane (1:5) as mobile phase to yield (2-bromo-5-phenoxyphenyl)methanol (4.7 g, 0.017 mol): RP-HPLC (Hypersil C18, 5 μm, 250×4.6 mm; 25%-100% over 10 min with 0.1 M ammonium acetate, 1 mL/min) Rt 11.7 min. TLC (ethyl acetate/heptane 1:5) Rf 0.18.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06660744B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-e6881106d19a47819921a3fd29407149
출처 메모uspto-grants-2003_12