Cesium carbonate → HCID 86754149, compound
Reaction equation
C(=O)([O-])[O-].[Cs+:5].[Cs+].[C:7]([O:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)(=[O:18])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16]>O.CO>[C:7]([O:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)(=[O:18])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]([O-:17])=[O:16].[Cs+:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Aqueous cesium carbonate (1M, 6.3 ml) is added dropwise to a solution of benzyl hydrogen azelate (3.00 g, 10.77 mmol) in 75 ml water/methanol (1:15) until the pH reaches approximately 7, whereupon the solvent is removed under reduced pressure and the residue dried under vacuum overnight. The oily, yellowish semicrystalline residue is dispersed in dry dimethylformamide (50 ml) and evaporated to dryness in vacuo. This procedure is repeated twice, yielding an off-white crystalline product. The product is used without further characterization.
Workup
- customwhereupon the solvent is removed under reduced pressure
- customthe residue dried under vacuum overnight
- additionThe oily, yellowish semicrystalline residue is dispersed in dry dimethylformamide (50 ml)
- customevaporated to dryness in vacuo
- customyielding an off-white crystalline product
Sources & evidence
- ORD record
- ord-06791c47a9ff46fcb0e73cf1ef963160
- Source dataset
- uspto-grants-1999_07
- Patent number
- US05919753
Reaction notes
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