Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67342661 | HCID 67342661 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67344003 | HCID 67344003 | — |
Reaction Steps
To a solution of 1-[6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-propoxy-1-ol (280 mg, 1.0 mmol) in THF (2 mL) and toluene (4 mL) is added 1,1′-(azodicarbonyl)dipiperidine (ADDP, 376.8 mg, 1.49 mmol) at 0° C., followed by the addition of triphenylphosphine (391.6 mg, 1.49 mmol) and methyl 4-hydroxybenzoate (181.7 mg, 1.19 mmol). The reaction mixture is warmed up to room temperature and stirred overnight. The mixture is loaded on silica gel, eluted with hexanes with a gradient from 0% of ethyl acetate to 50% of ethyl acetate giving ethyl 4-{1-[6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-propoxy}-benzoate (350 mg). The ester product is taken into ethanol (4 mL), treated with sodium hydroxide (5N aqueous, 1 mL) for 3 h at 40° C. The mixture is concentrated, diluted with ethyl acetate, acidified with 5 N HCl (1.1 mL), extracted with ethyl acetate. The organic layers are dried and concentrated giving 4-{1-[6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-propoxy}-benzoic acid (345 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989457B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-d60ccdcfbd6e4555acd09346fc97bf48 |
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| Source note | uspto-grants-2011_08 |
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