Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 22101526 | HCID 22101526 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 17760595 | HCID 17760595 | 80.2% |
Reaction Steps
The 4-(4 -ethoxycarbonylpiperidino)-5-hydroxy-2,6,6-trimethyl-2-cyclohepten-1-one obtained in Example 24 (0.68 g, 2.1 millimoles) was dissolved in acetic acid (5 ml), 6N hydrochloric acid (2 ml) was added and the mixture was heated at 80° C. for 90 minutes. Concentration to dryness followed by washing with ethyl acetate gave 0.56 g (80.2%) of 4-(4 -carboxypiperidino)-5-hydroxy-2,6,6-trimethyl-2-cyclohepten-1-one hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849801 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-6c3caf1a701e4f77af0b57587be12f13 |
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| Source note | uspto-grants-1998_12 |
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