Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxymorphone | HCID 5284604 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 627484 | HCID 627484 | — |
| Product | Oxymorphone | HCID 5284604 | — |
| Product | beta-Oxymorphol | HCID 21779240 | — |
Reaction Steps
The crude Oxymorphone Base (267.7 g wet, 180.1 g dry basis) was transferred back to a clean 3000 mL reaction vessel and 1-propanol (321.6 g) was charged. The slurry was heated to 90±3° C. and stirred for 1.5 h. The temperature was lowered to 25±5° C. and stirred for 1 h. The batch was further cooled to 10±5° C. and stirred 1 h. The product was collected by filtration washing the cake with 1-propanol (10±5° C., 2×48.2 g) then drying under vacuum at 55±5° C. to give Oxymorphone Base (167.8 g, 83.3% yield, 99.9 area %, 6α-oxymorphol 0.11 area %, 6β-oxymorphol not detected).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120800B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-b69d4aead2744f77805804183feba95f |
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| Source note | uspto-grants-2015_09 |
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