Catechol → HCID 129760973, compound
Reaction equation
[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])[OH:2].[O-]CC.[Mg+2:12].[O-]CC>C1(C)C=CC=CC=1>[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[O-:4])[O-:2].[Mg+2:12]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
A solution of catechol (2.20 g, 20 mmol) and toluene (45 ml) was dehydrated by distilling 5 mL of the solution. Thereafter, 2.29 g (20 mmol) of magnesium(II) ethoxide was added to the solution while stirring. The mixed solution was refluxed for 1 hour, and then, while the distillation temperature was 100° 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-magnesium complex) was black in color. The yield amount was 2.57 g (19.5 mmol), and the yield percentage was 97%. Catechol-magnesium complex was dissolved into acetylacetone until saturated, and then filtered to be used as a coating liquid.
Workup
- distillationby distilling 5 mL of the solution
- temperatureThe mixed solution was refluxed for 1 hour
- customwas 100° 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
- dissolutionCatechol-magnesium complex was dissolved into acetylacetone until saturated, and
- filtrationthen filtered
Sources & evidence
- ORD record
- ord-a7ddfd779af94b9fb4afc15d21cf6003
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08445118B2
Reaction notes
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