Catechol → HCID 131730588, compound
Reaction equation
[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])[OH:2].C([O-])(=O)C.[Eu+3:13].C([O-])(=O)C.C([O-])(=O)C>C1(C)C(C)=CC=CC=1>[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[O-:4])[O-:2].[Eu+3:13].[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[O-:4])[O-:2].[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[O-:4])[O-:2].[Eu+3:13]Participants
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
A solution of catechol (3.30 g, 30 mmol) and xylene (45 ml) was dehydrated by distilling 5 mL of the solution. Thereafter, 6.58 g (20 mmol) of europium acetate was added to the solution while stirring. The mixed solution was refluxed for 1 hour, and then, while the distillation temperature was 132° C. or higher, distilled until the amount of the solution became half. After the distillation, solid content of the product was isolated by suction filtering using a membrane suction filter. The residual solid content was heated to 100° C. under vacuum using a vacuum dryer so that remaining volatile components were completely removed. The solid content (catechol-europium complex) was yellow in color. The yield amount was 6.28 g (20 mmol), and the yield percentage was 100%. 0.314 g of catechol-europium complex was dissolved into 10 mL of acetylacetone/toluene to produce a coating liquid.
Workup
- distillationby distilling 5 mL of the solution
- temperatureThe mixed solution was refluxed for 1 hour
- customwas 132° C.
- distillationhigher, distilled until the amount of the solution
- distillationAfter the distillation, solid content of the product
- customwas isolated by suction
- filtrationfiltering
- filtrationfilter
- customwere completely removed
- dissolution0.314 g of catechol-europium complex was dissolved into 10 mL of acetylacetone/toluene
- customto produce a coating liquid
Sources & evidence
- ORD record
- ord-6ef22c3d9ef4405891d20b5e67238855
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08445118B2
Reaction notes
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