Hydrochloric Acid → HCID 20316401, compound
Reaction equation
[C:1]([C:3]1[C:8]([O:9][CH3:10])=[C:7]([O:11][CH3:12])[CH:6]=[CH:5][N:4]=1)#N.[OH-:13].[K+].Cl.[OH2:16]>>[CH3:10][O:9][C:8]1[C:3]([C:1]([OH:16])=[O:13])=[N:4][CH:5]=[CH:6][C:7]=1[O:11][CH3:12]Participants
5
Procedure
1 g of 3,4-dimethoxy-2-cyanopyridine obtained in Example e) and 3.5 g of potassium hydroxide in 15 ml of water are heated to 85° C. for half an hour. It is allowed to cool and in an ice bath hydrochloric acid is added gently to pH=2-3. After concentration to dryness, the residue is extracted three times with hot methanol, allowed to cool, filtered and concentrated. There is obtained a solid used crude.
Workup
- additionis added gently to pH=2-3
- concentrationAfter concentration to dryness
- extractionthe residue is extracted three times with hot methanol
- temperatureto cool
- filtrationfiltered
- concentrationconcentrated
- customThere is obtained a solid used crude
Sources & evidence
- ORD record
- ord-db39a970a5d344c38f5f9a96ea430995
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07560565B2
Reaction notes
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