Acetic Anhydride → Furo[3,4-b]pyridine-5,7-dione, 3-ethyl-
Reaction equation
[CH2:1]([C:3]1[CH:4]=[C:5]([C:12]([OH:14])=[O:13])[C:6]([C:9]([OH:11])=O)=[N:7][CH:8]=1)[CH3:2].C(OC(=O)C)(=O)C>>[CH2:1]([C:3]1[CH:4]=[C:5]2[C:12](=[O:13])[O:14][C:9](=[O:11])[C:6]2=[N:7][CH:8]=1)[CH3:2]Participants
3
Procedure
A mixture of the above carboxylic acid (3.0 g, 15.37 mmol) and acetic anhydride (15 ml) is heated until the acid is dissolved. The mixture is then concentrated under vacuum, and the residue is dissolved in ether, stirred, filtered, concentrated and dried to give 5-ethyl-2,3-pyridinedicarboxylic anhydride.
Workup
- temperatureis heated until the acid
- dissolutionis dissolved
- concentrationThe mixture is then concentrated under vacuum
- dissolutionthe residue is dissolved in ether
- filtrationfiltered
- concentrationconcentrated
- customdried
Sources & evidence
- ORD record
- ord-d82fc0977ebc4fc68d0126da10d28e86
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05098462
Reaction notes
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