Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 66611240 | HCID 66611240 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66611936 | HCID 66611936 | — |
Reaction Steps
To a solution of phenylmethyl 2-[(phenylmethyl)oxy]-4-(1-piperidinylcarbonyl)-5-(trifluoromethyl)benzoate (may be prepared as described in Description 57; 170 mg, 0.34 mmol) in tetrahydrofuran (4 ml) was added LiOH (24.55 mg, 1.03 mmol) and water (1 ml). The solution was heated at 45° C. for one hour then room temperature for 18 hours. 2M hydrochloric acid (0.51 ml, 1.03 mmol) was added and the solvent removed in vacuo. The residue was partitioned between ethyl acetate (20 ml) and 2M HCl (10 ml). The organic layer was separated, dried (MgSO4) and the solvent removed in vacuo to give the title compound. 139 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365551B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-48259f190f52495ca71e096ba7102b76 |
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| Source note | uspto-grants-2016_06 |
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