Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | L-Methionine | HCID 6137 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 3(3-Methoxyphenyl)-N,N,2-trimethyl pentane-1-amine, (2R,3R)- | HCID 11253328 | — |
| Solvent | Methylcyclohexane | HCID 7962 | — |
| Product | Tapentadol | HCID 9838022 | 89.5% |
Reaction Steps
18.9 kg of methanesulfonic acid and 2458 g D,L methionine were placed in methyl cyclohexane and then 3192 g (2R,3R)-[3-(3-methoxy-phenyl)-2-methyl-pentyl]-dimethylamine were added and the mixture was stirred at 82° C. for 18 hours. Subsequently, dilution was carried out with 10.3 l water at a maximum of 80° C. and 9 l methyl cyclohexane were added. At a maximum of 42° C., 17.3 l ammoniac were added until the pH was 8.8. A phase separation took place at 45° C. and 3.2 g (1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol were added to the organic phase at 40° C. and stirred for 1 hour at 36° C. Subsequently, after cooling slowly to 5° C. and a further hour of stirring, the precipitate which formed was extracted by suction, washed with 12 l methyl cyclohexane and dried in a drying chamber. 2685 g (89.5%) (1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol were obtained in modification B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08134032B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-3a1c836cbeee4b5a93f69b14b95b1075 |
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| Source note | uspto-grants-2012_03 |
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