HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043869Generated: October 31, 2026
Hydrochloric Acid → Oxymorphone Hydrochloride
https://huagongshe.com/reaction/1043869
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Oxymorphone | HCID 5284604 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Oxymorphone Hydrochloride | HCID 5359390 | — |
Reaction Steps
Oxymorphone free base (5.0027 g) was combined with water (2.5 mL) and 2-propanol (6.0 mL) in a round bottom flask (250 mL). The resulting mixture was heated in a temperature controlled bath, with stirring, from ambient to 60° C. over a time period of approximately 30 minutes. Concentrated hydrochloric acid (1.8 mL) was added with continued stirring. The temperature was increased to 70° C. resulting in a clear solution and then cooled to 60° C. 2-propanol was added in 3-5 mL aliquots over approximately 5 minute time span. Solids were observed after the addition of the second aliquot. The resulting slurry was cooled from 60 to 5° C. over 190 minutes and stirred at 5° C. for 45 minutes. Tan solids in a brown solution were observed. The flask was removed from the bath, the contents were vacuum filtered and the solids rinsed 5 times with 1 mL aliquots of 2-propanol:water (9:1 v:v). The resulting white solids were allowed to air-dry for 2 days to yield Form B oxymorphone HCl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563571B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-aa437aa4aa914b628eeb81da51943844 |
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| Source note | uspto-grants-2013_10 |
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