Salicylic Acid → HCID 90473079, compound
Reaction equation
C(=O)([O-])[O-].[Sr+2:5].[C:6]([OH:15])(=[O:14])[C:7]1[C:8](=[CH:10][CH:11]=[CH:12][CH:13]=1)[OH:9]>O>[C:6]([O-:15])(=[O:14])[C:7]1[C:8](=[CH:10][CH:11]=[CH:12][CH:13]=1)[OH:9].[Sr+2:5].[C:6]([O-:15])(=[O:14])[C:7]1[C:8](=[CH:10][CH:11]=[CH:12][CH:13]=1)[OH:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of strontium carbonate (1.0 g, 6.77 mmol) and salicylic acid (1.87 g, 13.5 mmol) in water (25 ml) was stirred for 4 hours. The solution became pale yellow and almost clear. The solution was filtered at room temperature and the filtrate was evaporated to dryness and dried in vacuo at ambient temperature. The title compound was isolated as a pale red powder. Yield 2.1 g (86%). Melting point above 300° C.
Workup
- filtrationThe solution was filtered at room temperature
- customthe filtrate was evaporated to dryness
- customdried in vacuo at ambient temperature
Sources & evidence
- ORD record
- ord-44911f7892364f0ab92488a5b362ad4a
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07241460B2
Reaction notes
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