Hydrochloric Acid → 4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-methyl-
Reaction equation
C([O:4][C:5]1[CH:14]=[C:13]([O:15]C(=O)C)[CH:12]=[C:11]2[C:6]=1[C:7](=[O:23])[C:8](C(=O)C)=[C:9]([CH3:19])[O:10]2)(=O)C.Cl>C(=O)([O-])[O-].[Na+].[Na+]>[OH:4][C:5]1[CH:14]=[C:13]([OH:15])[CH:12]=[C:11]2[C:6]=1[C:7](=[O:23])[CH:8]=[C:9]([CH3:19])[O:10]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5,7-Diacetoxy-3-acetyl-2-methylchromen-4-one is refluxed for 1 hour with 40 ml of 10% sodium carbonate solution. After cooling, the suspension is adjusted to a pH of about 6 using 2N HCl and cooled. The precipitate is filtered off, giving 0.6 g of very pale brown powder (TM=279.9° C.)
Workup
- temperatureAfter cooling
- temperaturecooled
- filtrationThe precipitate is filtered off
- customgiving 0.6 g of very pale brown powder (TM=279.9° C.)
Sources & evidence
- ORD record
- ord-2716593bf189409da9964b77bc278336
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09044409B2
Reaction notes
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