3-Chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid → 3-Chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid anhydride
Reaction equation
[Cl:1][C:2]1[C:6]2=[N:7][C:8]([C:14]([OH:16])=[O:15])=[C:9]([C:11]([OH:13])=O)[CH:10]=[C:5]2[S:4][CH:3]=1>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[C:6]2=[N:7][C:8]3[C:14](=[O:15])[O:16][C:11](=[O:13])[C:9]=3[CH:10]=[C:5]2[S:4][CH:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
3-Chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid (1.45 g) is heated at 85° to 90° C. for 30 minutes then 90° to 102° C. for 30 minutes in acetic anhydride (7 mL). The reaction is cooled, the solids filtered off and washed with ether to give 1.2 g of 3-chlorothieno[3,2-b]pyridine-5,6-dicarboxylic acid anhydride.
Workup
- temperatureThe reaction is cooled
- filtrationthe solids filtered off
- washwashed with ether
Sources & evidence
- ORD record
- ord-24a4383e93384db7ad8003169c2066e7
- Source dataset
- uspto-grants-1986_08
- Patent number
- US04608079
Reaction notes
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