Hydrochloric Acid → 2-(2,6-Diethyl-4-methylphenyl)-5-([1,3]dioxolan-2-ylmethyl)cyclohexane-1,3-dione

HRID 1027369

反応式

HRID 1027369 の反応式
[IH2+].[CH2:2]([C:4]1[CH:9]=[C:8]([CH3:10])[CH:7]=[C:6]([CH2:11][CH3:12])[C:5]=1B(O)O)[CH3:3].[OH2:16].[OH-:17].[Li+].Cl.C[O:21][CH2:22][CH2:23][O:24][CH3:25]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH2:2]([C:4]1[CH:9]=[C:8]([CH3:10])[CH:7]=[C:6]([CH2:11][CH3:12])[C:5]=1[CH:7]1[C:8](=[O:16])[CH2:9][CH:4]([CH2:2][CH:25]2[O:21][CH2:22][CH2:23][O:24]2)[CH2:5][C:6]1=[O:17])[CH3:3]

参加物

9

反応条件

温度
55 °C

実験手順

The iodonium ylide (477 mg, 1.19 mmol) prepared in Step 3a is added to a mixture of 2,6-diethyl-4-methylphenylboronic acid (343 mg, 1.79 mmol), tetrabutylammonium bromide (385 mg, 1.19 mmol), lithium hydroxide monohydrate (151 mg, 3.57 mmol) and palladium (II) acetate (13 mgs) in a mixture of 1,2-dimethoxyethane (10.8 ml) and water (2.7 ml) and the reaction mixture is heated at 55° C. for 5 hours. The reaction is then cooled, dilute aqueous hydrochloric acid is added, and the mixture is extracted with ethyl acetate. The organic extracts are combined, washed with water, dried over anhydrous magnesium sulfate, filtered and the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel to give 2-(2,6-diethyl-4-methylphenyl)-5-([1,3]dioxolan-2-ylmethyl)cyclohexane-1,3-dione

後処理

  1. temperatureThe reaction is then cooled
  2. extractionthe mixture is extracted with ethyl acetate
  3. washwashed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationthe filtrate is concentrated in vacuo
  7. customThe residue is purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-092fb6cee83243338803759582fbd833
出典データセット
uspto-grants-2014_05
特許番号
US08735322B2

関連ノート

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