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HRID 25107생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/25107

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-Butyn-1-OLHCID 13566—
반응물1-Bromo-2,4-dimethoxybenzeneHCID 87266—
촉매Palladium ChlorideHCID 24290—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DiethylamineHCID 8021—
생성물4-(2,4-Dimethoxyphenyl)-but-3-yn-1-olHCID 2256612744.3%

반응 조건

온도55 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858614B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-78783d950e6d48a0a4de70618ba60127
출처 메모uspto-grants-2005_02