HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Hydroxy-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 6-Methoxy-1-Indanone | HCID 334036 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 6-Hydroxy-1-indanone | HCID 7020659 | 80.6% |
Reaction Steps
Under argon atmosphere, 6-methoxy-1-indanone (10.0 g) was dissolved in xylene (100 ml), and to the mixture was added aluminum chloride (16.4 g). The mixture was refluxed for 2 hours and then cooled to room temperature. To the mixture was added 3N hydrochloric acid (100 ml), and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate) to give 6-hydroxy-1-indanone (7.36 g) as pale brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172061B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-65c632f23d5c4ec4adcdb83d4b44d6d5 |
| Source note | uspto-grants-2001_01 |