Carbonate Ion → HCID 68982944, compound

HRID 478613Notes

Reaction equation

HRID 478613 reaction equation
[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:12]=[CH:11][C:8]([O:9][CH3:10])=[C:6]([OH:7])[CH:5]=1.C(=O)([O-])[O-].O([CH2:26][C:27]([F:30])([F:29])[F:28])S(C(F)(F)F)(=O)=O>CN(C=O)C.C(Cl)Cl>[CH3:10][O:9][C:8]1[CH:11]=[CH:12][C:4]([C:3]([O:2][CH3:1])=[O:13])=[CH:5][C:6]=1[O:7][CH2:26][C:27]([F:30])([F:29])[F:28]

Participants

6

Procedure

To a mixture of isovanillic acid methyl ester (33.0 g, 0.18 mol) and potassiuin carbonate (41.4 g, 0.30 mol) in DMF (100 ml) was added a solution of trifluoroethyl triflate [Burdon et al Tetrahedron 21, 1 (1965)] (65.0 g, 0.28 mol) in CH2Cl2. The mixture was stirred at room temperature for 18 h then evaporated to 50 ml, the mixture partitioned between ether and H2O, the organic layer washed with H2O and saturated brine, then dried over MgSO4 and evaporated. The resulting solid was triturated with hexane to give the subtitle compound as an off-white solid (42.55 g, 90%). Rf 0.47 (CH2Cl2). MS m/z 265 (MH+).

Workup

  1. customthen evaporated to 50 ml
  2. customthe mixture partitioned between ether and H2O
  3. washthe organic layer washed with H2O and saturated brine
  4. dry with materialdried over MgSO4
  5. customevaporated
  6. customThe resulting solid was triturated with hexane

Sources & evidence

ORD record
ord-82e594685cea43b9921416971458cfde
Source dataset
uspto-grants-2003_11
Patent number
US06642242B2

Reaction notes

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