Hydrochloric Acid → HCID 54106909, compound
Reaction equation
[OH:1][C:2]1[CH:12]=[CH:11][C:5]2[C:6](=[O:10])[CH:7]=[CH:8][O:9][C:4]=2[CH:3]=1.[CH3:13][O:14][C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][C:22]=1[O:23][CH3:24])[CH:18]=O.Cl.CO>O>[CH3:13][O:14][C:15]1[CH:16]=[C:17]([CH:18]=[C:7]2[C:6](=[O:10])[C:5]3[CH:11]=[CH:12][C:2]([OH:1])=[CH:3][C:4]=3[O:9][CH2:8]2)[CH:20]=[CH:21][C:22]=1[O:23][CH3:24]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
After 7-hydroxy-4(4H)-benzopyranone 1.0 g and 3,4-dimethoxybenzaldehyde 1.22 g were added to a mixture of concentrated hydrochloric acid 50 ml and methanol 40 ml, the mixture was refluxed for 1.5 hours and cooled to room temperature, water 100 ml was added and the mixture was allowed to stand for 30 minutes. The precipitated crystals were filtered.
Workup
- temperaturethe mixture was refluxed for 1.5 hours
- filtrationThe precipitated crystals were filtered
Sources & evidence
- ORD record
- ord-84683e2b0b38484f9aedc0f5660e8ab3
- Source dataset
- uspto-grants-2000_06
- Patent number
- US06080781
Reaction notes
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