Toluene → 4-(5-Bromo-2-chlorophenyl)-2,2,6,6-tetramethylpyran-3,5-dione

HRID 1470878ノート

反応式

HRID 1470878 の反応式
[CH3:1][C:2]1([CH3:12])[C:7](=[O:8])[CH2:6][C:5](=[O:9])[C:4]([CH3:11])([CH3:10])[O:3]1.C(Cl)(Cl)Cl.C1(C)C=CC=CC=1.C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C.[Br:36][C:37]1[CH:38]=[CH:39][C:40]([Cl:44])=[C:41]([Pb+3])[CH:42]=1>ClCCl.Cl>[Br:36][C:37]1[CH:42]=[CH:41][C:40]([Cl:44])=[C:39]([CH:6]2[C:7](=[O:8])[C:2]([CH3:12])([CH3:1])[O:3][C:4]([CH3:11])([CH3:10])[C:5]2=[O:9])[CH:38]=1

参加物

7

反応物 4

HCID 1140TolueneHCID 6212ChloroformHCID 199092752,2,6,6-Tetramethyloxane-3,5-dioneHCID 178476543[Diacetyloxy-(5-bromo-2-chlorophenyl)plumbyl] acetate

生成物 1

HCID 684878854-(5-Bromo-2-chlorophenyl)-2,2,6,6-tetramethylpyran-3,5-dione収率 7.5%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 6344Dichloromethane溶媒

反応条件

温度
80 °C

実験手順

To a mixture of 2,2,6,6-tetramethylpyran-3,5-dione (2.78 g, 16.3 mmol) and N,N-dimethylaminopyridine (9.97 g, 81.6 mmol) is added anhydrous chloroform (120 ml). To this solution is added anhydrous toluene (30 ml), followed by 5-bromo-2-chlorophenyllead triacetate (10.32 g, 18 mmol) in one portion and the reaction mixture is heated at 80° C. overnight. The mixture is allowed to cool to room temperature, then diluted with dichloromethane (120 ml) and 2M aqueous hydrochloric acid (250 ml), followed by filtration through diatomaceous earth to remove inorganic residues. The filter cake is washed with dichloromethane, and all organic fractions are combined, washed with 2M hydrochloric acid, water and brine, dried over anhydrous magnesium sulfate then concentrated in vacuo. This material is finally purified by flash column chromatography on silica gel to afford 4-(5-bromo-2-chlorophenyl)-2,2,6,6-tetramethylpyran-3,5-dione (0.44 g) of sufficient purity to use directly in the next step.

後処理

  1. temperatureto cool to room temperature
  2. filtrationfollowed by filtration through diatomaceous earth
  3. customto remove inorganic residues
  4. washThe filter cake is washed with dichloromethane
  5. washwashed with 2M hydrochloric acid, water and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationthen concentrated in vacuo
  8. customThis material is finally purified by flash column chromatography on silica gel

出典と根拠

ORDレコード
ord-45c50dba1e324181b3463c018d2eb863
出典データセット
uspto-grants-2015_04
特許番号
US09006429B2

反応ノート

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