Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14987155 | HCID 14987155 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 14987156 | HCID 14987156 | — |
Reaction Steps
A suspension of cis-1-methoxycarbonyl-3-methyl-4-[(1-oxo-propyl)-2-fluorophenylamino]-piperidine (3.2 g, 9.89 mmol) in 48% aqueous HBr (20 ml) is refluxed for two hours. Upon heating the mixture dissolution occurs. The solution is cooled to 0° C. and 5N NaOH is added until the pH is between 11 and 12. The aqueous phase is extracted with methylene chloride (5×) and the combined organics dried over sodium sulfate and concentrated to give cis-3-methyl-4-(2-fluorophenylamino)-piperidine as an oil: 2.0 g; 97%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05019583 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-727298684b4b44fca66d0e4f9ad708dd |
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| Source note | uspto-grants-1991_05 |
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