Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 86646769 | HCID 86646769 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57467463 | HCID 57467463 | — |
Reaction Steps
To a solution of Example 48A (0.44 g, 1.4 mmol) in methanol (4 mL) and water (4 mL) was added 5 N aqueous NaOH solution (1.4 mL, 7.1 mmol). After stirring at 60° C. for 16 hours, the reaction mixture was cooled, neutralized to pH˜7 with 3 N HCl, and concentrated to obtain crude 2-[(1S,5R,6S)-6-(4-chlorophenyl)-3-azabicyclo[3.2.0]hept-3-yl]-2-methylpropanoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507493B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-a46ace6e74da4cefbbfa4a65d3b6c919 |
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| Source note | uspto-grants-2013_08 |
|---|