Hydroquinone → HCID 67586879, compound
Reaction equation
[C:1]([C:4]1([OH:19])[CH:12]=[CH:11][C:10]([NH:13][C:14](=[O:18])[C:15]([CH3:17])=[CH2:16])=[CH:9][CH:5]1[C:6]([OH:8])=[O:7])(=[O:3])[CH3:2].[C:20]1(C=CC(O)=CC=1)O.S(=O)(=O)(O)O>CO>[C:1]([C:4]1([OH:19])[CH:12]=[CH:11][C:10]([NH:13][C:14](=[O:18])[C:15]([CH3:17])=[CH2:16])=[CH:9][CH:5]1[C:6]([O:8][CH3:20])=[O:7])(=[O:3])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-acetyl-5-methacrylamidosalicylic acid and 1% by weight of hydroquinone in methanol was added 0.5% by weight of concentrated sulfuric acid, and the solution was subject to reflux for several hours. After evaporating the solvent, the remaining residue was recrystallized by a mixture of water and methanol to give methyl 2-acetyl-5-methacrylamidosalicylate.
Workup
- temperatureto reflux for several hours
- customAfter evaporating the solvent
- customthe remaining residue was recrystallized by a mixture of water and methanol
Sources & evidence
- ORD record
- ord-0a289d3f55614c0ab8a090437d8b3544
- Source dataset
- uspto-grants-1997_12
- Patent number
- US05693320
Reaction notes
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