Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-(Methoxymethoxy)benzaldehyde | HCID 250074 | — |
| Reactant | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67403470 | HCID 67403470 | 96% |
Reaction Steps
4-Methoxymethoxybenzaldehyde (658 mg, 3.96 mmol) was dissolved in tetrahydrofuran (4.0 mL). To this, (trifluoromethyl)trimethylsilane (702 μL, 475 mmol) and tetrabutylammonium fluoride (a 1.0 mol/L solution in tetrahydrofuran, 396 μL, 0.396 mmol) were added under a nitrogen atmosphere at 0° C. and the mixture was stirred at room temperature for 1 hour. To the reaction mixture, tetrabutylammonium fluoride (a 1.0 mol/L solution in tetrahydrofuran, 4.00 mL, 4.00 mmol) was added and the mixture was further stirred for 10 minutes. After water was added to the reaction mixture, extraction with ethyl acetate was performed, followed by washing with brine and drying over anhydrous sodium sulfate. The solvent was evaporated off under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=7/3) to give 1-methoxymethoxy-4-(2,2,2-trifluoro-1-hydroxyethyl)benzene (Compound CQ) (895 mg, yield: 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673908B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-c410e1c8944f4aceaec27561f69355e7 |
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| Source note | uspto-grants-2014_03 |
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