Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 10528708 | HCID 10528708 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 45264916 | HCID 45264916 | 44% |
Reaction Steps
(R)-1-(2-((2,2-bis(4-Fluoro-2-methylphenyl)ethenyl)oxy)ethyl)-3-piperidinecarboxylic acid ethyl ester (1.72 g, 0.0039 mol, prepared similarly to the method described in Example 70) was dissolved in ethanol (20 ml) and 10 N sodium hydroxide solution (4 ml) was introduced. The solution was stirred at room temperature for 3 h and water (100 ml) was added. The solution was extracted with diethyl ether (2×100 ml) and the aqueous phase was acidified to pH 5 with 2 N hydrochloric acid solution. Extraction with dichloromethane (4×80 ml) and drying of the combined extracts (MgSO4) followed by evaporation gave a residue, which was dissolved in toluene (50 ml). Methanol (0.16 ml) and chlorotrimethylsilane (0.51 ml) were added, and the product precipitated. The mixture was evaporated to a solid and recrystallized from toluene to give the title compound as a white crystalline solid (0.78 g, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174898B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-ac69442448d44e49abf580136fbc77ea |
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| Source note | uspto-grants-2001_01 |
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