Sodium Carbonate → 3-(4-Bromo-3,5-dimethylphenyl)furan

HRID 237581ノート

反応式

HRID 237581 の反応式
[Br:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5](Br)=[CH:4][C:3]=1[CH3:10].C([O-])([O-])=O.[Na+].[Na+].[O:17]1[CH2:22][CH2:21]O[CH2:19][CH2:18]1>>[Br:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([C:19]2[CH:21]=[CH:22][O:17][CH:18]=2)=[CH:4][C:3]=1[CH3:10]

参加物

4

反応条件

温度
100 °C

実験手順

A mixture of 2,5-dibromo-1,3-dimethylbenzene (2.00 g), 1-furan-3-ylboronic acid (856 mg), and 2 M aqueous Na2CO3 solution (11 mL) in 1,4-dioxane (40 mL) is purged with argon for 5 min. Tetrakis-triphenylphosphine-palladium-(0) (270 mg) is added and the mixture is stirred at 100° C. over night. More tetrakis-triphenylphosphine-palladium-(0) (50 mg) is added and the mixture is stirred for another 5 h at 100° C. After cooling to room temperature the mixture is diluted with ethyl acetate and aqueous NH4Cl solution. The aqueous phase is extracted with ethyl acetate and the combined extracts are washed with brine, dried over MgSO4 and concentrated in vacuo. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 100:0→90:10) to give the title compound. LC (method 7): tR=1.22 min; Mass spectrum (EI+): m/z=250 [M]+.

後処理

  1. customis purged with argon for 5 min
  2. additionTetrakis-triphenylphosphine-palladium-(0) (270 mg) is added
  3. additionMore tetrakis-triphenylphosphine-palladium-(0) (50 mg) is added
  4. stirringthe mixture is stirred for another 5 h at 100° C
  5. temperatureAfter cooling to room temperature the mixture
  6. additionis diluted with ethyl acetate and aqueous NH4Cl solution
  7. extractionThe aqueous phase is extracted with ethyl acetate
  8. washthe combined extracts are washed with brine
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated in vacuo
  11. customThe residue is chromatographed on silica gel (cyclohexane/ethyl acetate 100:0→90:10)

出典と根拠

ORDレコード
ord-f154be457bf6438aa528ccb3f64bc831
出典データセット
uspto-grants-2014_02
特許番号
US08642585B2

反応ノート

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