HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256126Generated: October 30, 2026
Acetone → Furo[2,3-b]pyridine-5,6-dicarboxylic acid
https://huagongshe.com/reaction/256126
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diethyl furo[2,3-b]pyridine-5,6-dicarboxylate | HCID 13849598 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Furo[2,3-b]pyridine-5,6-dicarboxylic acid | HCID 13752512 | — |
Reaction Steps
Potassium hydroxide (5.60 g, 85%, 0.087 mol) in water (5 mL) is added to a stirred suspension of diethyl furo[2,3-b]pyridine-5,6-dicarboxylate (9.3 g, 0.035 mol) in absolute ethanol (100 mL). The reaction mixture is heated at 60° C. for one hour, then cooled and anhydrous acetone added. The precipitate is filtered off, dried, suspended in dry acetone and treated with hydrogen chloride to adjust to a pH of 2. Crystallization of the isolated solids from an ethyl acetate-acetone mixture affords furo[2,3-b]pyridine-5,6-dicarboxylic acid mp 189°-192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04701208 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-9ab321f4b2904f979383caab30533fae |
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| Source note | uspto-grants-1987_10 |
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