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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720845생성일: 2026년 10월 25일

Triethylamine → 3-[4-[(6-Bromohexyl)oxy]but-1-ynyl}benzenesulfonamide

https://huagongshe.com/reaction/720845

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Bromobenzene-1-sulfonamideHCID 2734765—
반응물6-Bromohexylbut-3-ynyl etherHCID 11379281—
촉매TriphenylphosphineHCID 11776—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매TetrahydrofuranHCID 8028—
생성물3-[4-[(6-Bromohexyl)oxy]but-1-ynyl}benzenesulfonamideHCID 2189555890.7%

반응 조건

온도50 °C

반응 단계

A mixture of 3-bromo-benzenesulfonamide (625 g), 6-bromohexyl but-3-ynyl ether (850.1 g), bis(triphenylphosphine)palladium (II) chloride (62.5 g), triphenylphosphine (18.1 g) and triethylamine (536.3 g) in tetrahydrofuran (6250 ml) was stirred under an atmosphere of nitrogen for 20 mins. Copper (I) iodide (12.5 g) was then added to give a dark red/brown mixture that was heated to 50° C. for 23 h. The reaction mixture was then cooled to room temperature and filtered through a short silica pad (1000 g). The pad was washed with additional tetrahydrofuran (15.6 L) and the resulting solution then concentrated under reduced pressure to give crude product (1382 g) as a viscous oil. This was purified by chromatography (7 kg silica) eluting with 5:1 petroleum ether:ethyl acetate followed by 2:1 petroleum ether:ethyl acetate to give the title compound (932.9 g) as an oil, LC RT=5.69 min, δ (DMSO-d6) 7.79 (1H, s), 7.76 (1H, d, J 7.6 Hz), 7.56 (2H, m), 7.42 (2H, m), 3.55 (2H, t, J 6.6 Hz), 3.49 (2H, t, J 6.6 Hz), 3.42 (2H, t, J 6.6 Hz), 2.68 (2H, t, J 6.6 Hz), 1.76 (2H, m), 1.50 (2H, m), 1.35 (4H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135600B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-89789490575441eb9773dc2d93502ab3
출처 메모uspto-grants-2006_11