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Potassium Carbonate → 3-Phenyl-2,4-heptanedione

HRID 891070
ノート
印刷プレビュー

反応式

HRID 891070 の反応式
[CH3:1][C:2](=[O:10])[CH2:3][C:4](=[O:9])[CH2:5][CH2:6][CH2:7]C.I[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(=O)([O-])[O-].[K+].[K+]>CS(C)=O.[Cu]I>[C:12]1([CH:3]([C:4](=[O:9])[CH2:5][CH2:6][CH3:7])[C:2](=[O:10])[CH3:1])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 11430Potassium CarbonateHCID 11575IodobenzeneHCID 841922,4-Octanedione

生成物 1

HCID 222446113-Phenyl-2,4-heptanedione収率 48.7%

試薬・触媒・溶媒 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒HCID 679
Dimethyl Sulfoxide
溶媒

反応条件

温度
120 °C

実験手順

To a stirred mixture of 2,4-octanedione (568 mg, 4.0 mmol) and iodobenzene (408 mg, 2.0 mmol) in dimethylsulfoxide (10 mL) were added copper(I) iodide (380 mg, 2.0 mg) and potassium carbonate (1.10 g, 8.0 mmol). The mixture was heated at 120° C. for 4 h. The mixture was filtered through a pad of Celite and the filtrate was partitioned between ether and water. Organic layer was dried (Na2SO4) and the solvent was removed. The crude product was purified by TLC with hexane/ethyl acetate (4:1) to afford 199 mg (46%) of the title compound as colorless oil: 1H-NMR (CDCl3) δ 7.42-7.33 (3H, m), 7.18-7.15 (2H, m), 2.11 (2H, t, J=8.3 Hz), 1.87 (3H, s), 1.58-1.44 (3H, m), 1.25-1.16 (2H, m), 0.79 (3H, t, J=7.2 Hz).

後処理

  1. filtrationThe mixture was filtered through a pad of Celite
  2. customthe filtrate was partitioned between ether and water
  3. dry with materialOrganic layer was dried (Na2SO4)
  4. customthe solvent was removed
  5. customThe crude product was purified by TLC with hexane/ethyl acetate (4:1)

出典と根拠

ORDレコード
ord-785bbebae10540c7892a27c1dc122ae4
出典データセット
uspto-grants-2006_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07001917B2

反応ノート

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