HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium ethoxide → Furo(3,2-b)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Furo[3,2-b]pyridine-2-carboxylic acid | HCID 13803071 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Furo(3,2-b)pyridine | HCID 12210217 | — |
Reaction Steps
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))
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06630485B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-5c335d64479243f28bcb2ddaebd3e6fb |
| Source note | uspto-grants-2003_10 |