Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 15385774 | HCID 15385774 | — |
| Product | HCID 15385775 | HCID 15385775 | — |
Reaction Steps
4,5α-epoxy-6α-((5-methoxycarbonyl-valeryl)-oxy)-3-methoxymethoxy-17-methyl-morphinane (0.43 g, 0.91 mmol) was mixed with H2O (15 ml) and glacial acetic acid (15 ml) and stirred for 6 hours at 100° C. The mixture was then evaporated down at 40° C. using a Rotavapor and the residue obtained was purified by flash chromatography (60 g silical gel; CH2Cl2 /MeOH=9/1). The product was dissolved in H2O (6 ml) and glacial acetic acid (0.6 ml) and lyophilised. Yield: 0.221 g (0.45 mmol, 49.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150524 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-f962882be8954e96a31f6cdee28e97fa |
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| Source note | uspto-grants-2000_11 |
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