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HRID 25107作成日:2026年10月26日

Triphenylphosphine → 4-(2,4-Dimethoxyphenyl)-but-3-yn-1-ol

https://huagongshe.com/reaction/25107

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-Butyn-1-OLHCID 13566—
反応物1-Bromo-2,4-dimethoxybenzeneHCID 87266—
触媒Palladium ChlorideHCID 24290—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒DiethylamineHCID 8021—
生成物4-(2,4-Dimethoxyphenyl)-but-3-yn-1-olHCID 2256612744.3%

反応条件

温度55 °C

反応手順

1-Bromo-2,4-dimethoxybenzene (10 g 0.046 mol), palladium chloride (0.2 g 0.11 mmol) and triphenylphosphine (0.6 g 0.0023 mol) were dissolved in diethylamine (100 mL) under a nitrogen atmosphere. Copper (I) iodide (0.44 g 0.0023 mol) and 3-butyn-1-ol (7 mL 0.092 mol) were added into the reaction mixture at once. The mixture was stirred overnight at 55° C. under a nitrogen atmosphere. The catalyst was filtered off from the reaction mixture and the same amount of palladium chloride, triphenylphosphine, copper (I) iodide and 3-butyn-1-ol were added. The reaction mixture was stirred and heated at 85° C. for 48 hours. Then the solvent was removed at reduced pressure and water (approx. 100 mL) was added to the residue. The mixture was extracted with ethyl acetate (350 mL) passed through a pad of silica gel and concentrated. The product was purified by flash chromatography (silica gel, 1:1 hexanes/ethyl acetate). Compound 75 (4.2 g, 24%) was isolated as a brown oil. 1H NMR (300 MHz, CDCl3) δ2.24 (t, 1H), 2.73 (t, 2H), 3.80 (br s, 5H), 3.87 (s, 3H), 6.43 (m, 2H), 7.30 (m, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858614B2
出典データセットuspto-grants-2005_02
ORD IDord-78783d950e6d48a0a4de70618ba60127
出典メモuspto-grants-2005_02