Sodium ethoxide → Furo(3,2-b)pyridine
Reaction equation
[O-]CC.[Na+].C([C:8]1[O:16][C:15]2[C:10](=[N:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=1)(O)=O>C(O)C>[O:16]1[C:15]2[C:10](=[N:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[CH:8]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Reaction of 30 with ethyl bromoacetate in the presence of a non-nucleophilic base such as sodium hydride in a suitable organic solvent such as tetrahydrofuran gives a compound of formula 31. Treatment of 31 with base such as sodium ethoxide in ethanol, followed by thermolysis of the resulting 2-carboxyfuro[3,2-b]pyridine of formula 32 gives furo[3,2-b]pyridine of formula 33 ((see., Shiotani, S., and Moriata, H. J. Heterocyclic Chem., 23, 665 (1986))
Sources & evidence
- ORD record
- ord-d9d067b3b6774f0f822f94d01e90a444
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06316464B1
Reaction notes
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