Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Dihydrothebaine | HCID 5486617 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Hydrocodone | HCID 5284569 | 84.9% |
Reaction Steps
In this Example, 8,14-dihydro-thebaine (6.00 g, 19.14 mmol) was mixed with 24 ml of approx. 6 N Hydrochloric acid (144 mmol, prepared by mixing concentrated hydrochloric acid (12 ml) with DI water (12 ml)) at room temperature with stirring. The homogeneous light yellow colored solution was stirred for 4 hours. Thin Layer chromatography on silica gel plates 90:10:1 (dichloromethane:methanol: concentrated ammonium hydroxide) indicated that the reaction was complete. Decolorizing charcoal (Darco, 0.3 g) was added to the mixture and the reaction stirred for 20 minutes and then filtered. The charcoal was washed with DI water (2×5 ml). The combined acidic phases were cooled to <5° C. and the pH was adjusted to 9.64 with concentrated (28.0-30.0%) ammonium hydroxide solution (approx. 20 ml). The solid was filtered and washed with 2×10 ml of DI water. The product was dried at 60° C. under 22″ Hg vacuum until constant weight to give hydrocodone as a white amorphous said (4.87 g, 84.9% yield, 96.2 wt % by assay).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399671B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d15a77c7de60436f844f29866a9184d8 |
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| Source note | uspto-grants-2013_03 |
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