Triphenylphosphine → HCID 22566127、化合物

HRID 25107

反応式

HRID 25107 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[O:10][CH3:11].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH2:31]([OH:35])[CH2:32][C:33]#[CH:34]>C(NCC)C.[Pd](Cl)Cl.[Cu]I>[CH3:11][O:10][C:3]1[CH:4]=[C:5]([O:8][CH3:9])[CH:6]=[CH:7][C:2]=1[C:34]#[C:33][CH2:32][CH2:31][OH:35]

参加物

7

反応物 3

HCID 11776TriphenylphosphineHCID 135663-Butyn-1-OLHCID 872661-Bromo-2,4-dimethoxybenzene

生成物 1

HCID 22566127HCID 22566127、化合物収率 44.3%

試薬・触媒・溶媒 3

HCID 24290Palladium Chloride触媒HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒HCID 8021Diethylamine溶媒

反応条件

温度
55 °C

実験手順

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).

後処理

  1. filtrationThe catalyst was filtered off from the reaction mixture
  2. additionthe same amount of palladium chloride, triphenylphosphine, copper (I) iodide and 3-butyn-1-ol were added
  3. stirringThe reaction mixture was stirred
  4. temperatureheated at 85° C. for 48 hours
  5. customThen the solvent was removed at reduced pressure and water (approx. 100 mL)
  6. additionwas added to the residue
  7. extractionThe mixture was extracted with ethyl acetate (350 mL)
  8. concentrationconcentrated
  9. customThe product was purified by flash chromatography (silica gel, 1:1 hexanes/ethyl acetate)

出典と根拠

ORDレコード
ord-78783d950e6d48a0a4de70618ba60127
出典データセット
uspto-grants-2005_02
特許番号
US06858614B2

関連ノート

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