Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 14576914 | HCID 14576914 | — |
| Product | HCID 14576922 | HCID 14576922 | 80% |
Reaction Steps
To 1.00 g of 1-(4-chlorophenyl)-6-(4-hydroxyphenyl)-2-piperidone was added 25 ml of acetic anhydride and the mixture was stirred at 120° C. for 1 hour. The solvent was evaporated under reduced pressure and the residue was recrystallized from ethyl acetate to give 910 mg of 1-(4-chlorophenyl)-6-(4-acetoxyphenyl)-2-piperidone as colorless prisms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04839360 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-2fe68a267463413d994c495275dffb29 |
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| Source note | uspto-grants-1989_06 |
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