Hydrochloric Acid → HCID 54696200, compound
Reaction equation
Cl.[OH:2][C:3]1[CH:8]=[C:7]([CH3:9])[N:6]([CH2:10][C:11]([OH:13])=[O:12])[C:5](=[O:14])[C:4]=1[N+:15]([O-:17])=[O:16].[CH3:18]O>>[OH:2][C:3]1[CH:8]=[C:7]([CH3:9])[N:6]([CH2:10][C:11]([O:13][CH3:18])=[O:12])[C:5](=[O:14])[C:4]=1[N+:15]([O-:17])=[O:16]Participants
4
Procedure
250 ml of methanol are saturated with a gaseous hydrochloric acid stream and 25 g (0.11 mol) of 4-hydroxy-6-methyl-3-nitro-2-oxo-1,2-dihydropyridine-1-acetic acid are introduced in portions. The mixture is heated at reflux temperature for 4 hours and then the precipitate is filtered and it is dried in an oven. 23 g of product are obtained in the form of yellow crystals.
Workup
- additionare introduced in portions
- temperatureThe mixture is heated
- temperatureat reflux temperature for 4 hours
- filtrationthe precipitate is filtered
- customit is dried in an oven
Sources & evidence
- ORD record
- ord-47d318e66a824c00b53faf4c9e3cf548
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06252082B1
Reaction notes
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