2,4-Dihydroxybenzoic Acid → HCID 178524493, compound
Reaction equation
[Bi:1].[C:2]([OH:12])(=[O:11])[C:3]1[C:4](=[CH:6][C:7](=[CH:9][CH:10]=1)[OH:8])[OH:5]>>[C:2]([O-:12])(=[O:11])[C:3]1[C:4](=[CH:6][C:7](=[CH:9][CH:10]=1)[OH:8])[OH:5].[Bi+3:1].[C:2]([O-:12])(=[O:11])[C:3]1[C:4](=[CH:6][C:7](=[CH:9][CH:10]=1)[OH:8])[OH:5].[C:2]([O-:12])(=[O:11])[C:3]1[C:4](=[CH:6][C:7](=[CH:9][CH:10]=1)[OH:8])[OH:5]Participants
3
Conditions
- Temperature
- 50 °C
Procedure
In this process the β-resorcylic acid is dissolved in the hydroalcoholic medium with an increase in the temperature to a temperature of between approximately 40° C. and approximately 60° C., preferably approximately 50° C., and then a bismuth compound is added with stirring; the temperature is raised to a temperature of between approximately 70° C. and approximately 90° C., preferably approximately 80° C., allowing the reaction to continue, advantageously for between 2 and 15 hours, preferably approximately 5 hours. The suspension is filtered off, washed and dried. The product obtained corresponds to a bismuth β-resorcylate containing two bismuth atoms per molecule of acid.
Workup
- temperaturethe temperature is raised to a temperature of between approximately 70° C. and approximately 90° C., preferably approximately 80° C.
- customthe reaction
- filtrationThe suspension is filtered off
- washwashed
- customdried
Sources & evidence
- ORD record
- ord-cdcef2a60ff74c23a1861b8edcf7418e
- Source dataset
- uspto-grants-1997_06
- Patent number
- US05639987
Reaction notes
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