HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Diethyl furo[2,3-b]pyridine-5,6-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Diethyl 5-acetyl-1,6-dihydro-6-oxo-2,3-pyridinedicarboxylate | HCID 13752508 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Diethyl furo[2,3-b]pyridine-5,6-dicarboxylate | HCID 13849598 | — |
Reaction Steps
A xylene solution of the hydroxy-furo compound obtained in Example 61, (3.7 g) containing para-toluene sulfonic acid (0.01 g) is heated at reflux for two hours. The solution is cooled and the xylene solution decanted off. The residue is extracted with ether and the extracts combined with the xylene. Distillation of the solvents gives a yellow solid which is crystallized from a cyclohexane-toluene mixture to give pure diethyl furo[2,3-b]pyridine-5,6-dicarboxylate mp 66°-77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04608079 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-fd060fa844954e60b9786ee1f6276942 |
| Source note | uspto-grants-1986_08 |