Cesium carbonate → HCID 59442920, compound

HRID 1959140Notes

Reaction equation

HRID 1959140 reaction equation
[CH2:1]([C:3]1([CH2:29][CH3:30])[CH:12]=[C:11](OS(C(F)(F)F)(=O)=O)[C:10]2[C:5](=[CH:6][C:7]([O:21][Si](C(C)(C)C)(C)C)=[CH:8][CH:9]=2)[O:4]1)[CH3:2].[F:31][C:32]1[CH:37]=[CH:36][C:35](B(O)O)=[CH:34][CH:33]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>C(COC)OC.O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[F:31][C:32]1[CH:37]=[CH:36][C:35]([C:11]2[C:10]3[C:5](=[CH:6][C:7]([OH:21])=[CH:8][CH:9]=3)[O:4][C:3]([CH2:1][CH3:2])([CH2:29][CH3:30])[CH:12]=2)=[CH:34][CH:33]=1

Participants

6

Procedure

A mixture of the compound obtained in (3) described above (3.5 g), 4-fluorophenylboronic acid (1 g), cesium carbonate (12.7 g) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (350 mg, 10% wt) in dimethoxyethane/water (3/1; 60 mL) was heated under reflux under nitrogen atmosphere for 12 hours. The reaction solution was concentrated in vacuo, and the residue was extracted with ethyl acetate (40 ml×3). The combined organic layer was washed with saturated brine, dried over sodium sulfate, filtered and the filtrate was concentrated in vacuo. The residue is purified by column chromatography on silica gel (Solvent: petroleum ether/ethyl acetate=20/1) to give the titled compound (2 g) as a colorless powder.

Workup

  1. additionA mixture of the compound
  2. temperaturewas heated
  3. temperatureunder reflux under nitrogen atmosphere for 12 hours
  4. concentrationThe reaction solution was concentrated in vacuo
  5. extractionthe residue was extracted with ethyl acetate (40 ml×3)
  6. washThe combined organic layer was washed with saturated brine
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationthe filtrate was concentrated in vacuo
  10. customThe residue is purified by column chromatography on silica gel (Solvent: petroleum ether/ethyl acetate=20/1)

Sources & evidence

ORD record
ord-2b5622990c994a1788b07cabc7f6e153
Source dataset
uspto-grants-2013_04
Patent number
US08410166B2

Reaction notes

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