HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3,5-Dioxohexanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 6-Hydroxy-2-naphthoic acid | HCID 85557 | — |
| Reactant | Ethyl 6-hydroxy-2-naphthoate | HCID 2769636 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3,5-Dioxohexanoic acid | HCID 5459844 | — |
Reaction Steps
A solution of ethyl 6-hydroxyl-2-naphthate (49, 89 mg, 0.42 mmole) (6-hydroxy-2-naphthoic acid was obtained from TCI America and converted to the ester using standard esterification methods) and iodide (2, 177 mg, 0.42 mmole) in dimethylforamide (1 ml) was stirred with potassium carbonate (174 mg) for 14 hours. The reaction mixture was worked up with water (30 ml) and ethyl acetate (100 ml). The organic layer was washed with brine (30 ml), dried over sodium sulfate, filtered and concentrated. The crude product was purified on a silica gel column (hexane ethyl acetate, 4:1) to provide the triacetate of 3 (120 mg, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05837689 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-71a6bdb1d083416fa504b16cd48b587d |
| Source note | uspto-grants-1998_11 |