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HRID 2117674作成日:2026年10月27日

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

https://huagongshe.com/reaction/2117674

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Bromobenzene-1-sulfonamideHCID 2734765—
反応物6-Bromohexylbut-3-ynyl etherHCID 11379281—
触媒TriphenylphosphineHCID 11776—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒TetrahydrofuranHCID 8028—
生成物3-[4-[(6-Bromohexyl)oxy]but-1-ynyl}benzenesulfonamideHCID 2189555890.7%

反応条件

温度50 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07442719B2
出典データセットuspto-grants-2008_10
ORD IDord-7ac69d1e0f6542e4876d092764a4c431
出典メモuspto-grants-2008_10