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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1875164생성일: 2026년 10월 25일

({3-[(3-Bromo-5-chlorophenyl)oxy]-4-chloro-2-fluorophenyl}methyl)amine → ({3-[(3-Butyl-5-chlorophenyl)oxy]-4-chloro-2-fluorophenyl}methyl)amine

https://huagongshe.com/reaction/1875164

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참여 물질

역할이름HCID투입량
반응물({3-[(3-Bromo-5-chlorophenyl)oxy]-4-chloro-2-fluorophenyl}methyl)amineHCID 68487182—
반응물HCID 178448256HCID 178448256—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물({3-[(3-Butyl-5-chlorophenyl)oxy]-4-chloro-2-fluorophenyl}methyl)amineHCID 6848543775%

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온도60 °C

반응 단계

To a solution of ({3-[(3-bromo-5-chlorophenyl)oxy]-4-chloro-2-fluorophenyl}methyl)amine (300 mg, 0.822 mmol) and tetrakis(triphenylphosphine)palladium(0) (950 mg, 0.822 mmol) in THF (4 ml) was added n-butyl zinc bromide (0.5 M solution in THF) (1.644 ml, 0.822 mmol) and the reaction mixture was heated at 60° C. for one hour. The reaction mixture was diluted with EtOAc and washed with water. The solvent was removed and the crude material was purified via silica gel chromatography to give ({3-[(3-butyl-5-chlorophenyl)oxy]-4-chloro-2-fluorophenyl}methyl)amine (210 mg, 0.614 mmol, 75% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.43 (s, 2H), 6.97 (s, 1H), 6.68 (s, 1H), 6.64 (s, 1H), 3.71 (s, 2H), 2.50 (t, 2H), 1.88 (br. s., 2H), 1.45 (quin, 2H), 1.14-1.29 (m, 2H), 0.82 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08304419B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-b3fb5c0ec1c04ad8b8a17b7b1f0e60d6
출처 메모uspto-grants-2012_11