Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 67982732 | HCID 67982732 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67982825 | HCID 67982825 | 74.4% |
Reaction Steps
To a solution of tert-butyl(2-ethoxy-4-(3-phenylprop-1-enyl)phenoxy)-dimethylsilane (3.12 g, 8.46 mmol, 1.0 equiv.), in THF (17 mL), n-Bu4NF (10.2 mL, 10.2 mmol, 1.2 equiv., 1.0 M in THF) was added, and the mixture was stirred at 25° C. for 1 h. After addition of H2O, the aqueous layer was extracted with MTBE (2×), the combined organic phases were washed with brine, dried (MgSO4), filtered and the filtrate was concentrated. The residue was purified by flash chromatography on SiO2 (cyclohexane/EtOAc 95:5) to yield 1.60 g (74%) of the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193935B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-5a6ec16d3d6642db9522558b24b45c33 |
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| Source note | uspto-grants-2015_11 |
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