Salicylic Acid → HCID 178443019, compound
Reaction equation
[C:1]([OH:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[C:11]([O-:20])(=[O:19])[C:12]1[C:13](=[CH:15][CH:16]=[CH:17][CH:18]=1)[OH:14].[CH2:21]([N+:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36]>CC(C)=O>[C:1]([O-:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[CH2:21]([N+:37]1[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=1)[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36].[C:11]([OH:20])(=[O:19])[C:12]1[C:13](=[CH:15][CH:16]=[CH:17][CH:18]=1)[OH:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Salicylic acid (5-15 mmol) and cetylpyridinium salicylate (5 mmol) were dissolved in 20 ml of acetone and stirred for 15 min at room temperature. The solvent was evaporated and the remaining viscous liquid was dried at 0.1 mbar with stirring for 24 hrs.
Workup
- customThe solvent was evaporated
- customthe remaining viscous liquid was dried at 0.1 mbar
- stirringwith stirring for 24 hrs
Sources & evidence
- ORD record
- ord-063974fcfc2b46e7b5d5aa98b01f41ba
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09278134B2
Reaction notes
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