Hydrochloric Acid → HCID 21474381, compound
Reaction equation
[CH2:1]([C:8]1[N:9]([CH2:16][CH2:17][O:18]C(=O)C)[CH:10]=[CH:11][C:12](=[O:15])[C:13]=1[OH:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl>[OH-].[Na+].C(O)C>[CH2:1]([C:8]1[N:9]([CH2:16][CH2:17][OH:18])[CH:10]=[CH:11][C:12](=[O:15])[C:13]=1[OH:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
0.915 g of 2-benzyl-3-hydroxy-1-(2-acetoxy-ethyl)-1H-pyridin-4-one (Example 42) are stirred at room temperature in a mixture of 2 ml of 2N NaOH and 10 ml of ethanol for 24 hours. Then 2 ml of 2N HCl are added and the reaction mixture is stirred at room temperature for one hour, filtered and washed with cold ethanol. Drying yields 2-benzyl-3-hydroxy-1-(2-hydroxy-ethyl)-1H-pyridin-4-one.
Workup
- filtrationfiltered
- washwashed with cold ethanol
- customDrying
Sources & evidence
- ORD record
- ord-6d1f62f355e1475db1f0e16e99557b46
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05688815
Reaction notes
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