Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 58629833 | HCID 58629833 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86604664 | HCID 86604664 | — |
Reaction Steps
To a stirred solution of ethyl 3-{4-[(1-{6-[4-(trifluoromethyl)phenyl]-2-pyridinyl}pentyl)oxy]phenyl}propanoate (92 mg, 0.19 mmol) in THF (3 mL) and methanol (3 mL) was added, drop-wise, aqueous NaOH (2M, 3 mL). After 17 hours the mixture was concentrated under vacuum and the solid residue acidified with aqueous HCl (2M, 3.5 mL), diluted with water (10 mL) and extracted with DCM (2×10 mL). The combined organic layer was washed with brine (20 mL), dried (MgSO4) and concentrated under vacuum. The acid was loaded onto a PE-AX isolute SPE cartridge (pre-conditioned with 1 column volume of methanol) in 9 mL of methanol and a few drops of Et3N. The cartridge was washed with 3 column volumes of methanol followed by 10% aqueous HCl (2M) in methanol (2×5 mL) and 20% aqueous HCl (2M) in methanol (2×5 mL), yielding the title compound (38 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07338960B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-d778386ae16246149280d1d66fe397f8 |
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| Source note | uspto-grants-2008_03 |
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