Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 19426931 | HCID 19426931 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19426979 | HCID 19426979 | — |
Reaction Steps
Under N2 the compound from Step 1 (94 mg, 0.159 mmol) was dissolved in THF (2 mL). Tetrabutylammonium fluoride was added (795 μL, 0.795 mmol) and the reaction was stirred at 55° C. for 1 h. Ethyl acetate was added and the organic phase was washed with brine, dried over MgSO4, filtered and evaporated to give an oil which was purified by a flash silica column using EtOAc then 5% MeOH in CH2Cl2 as the eluent. The title compound was obtained: 12.8 mg (17%). Mass spec.: 461 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05527827 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-07af672d548c482db8a05a018e92ab93 |
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| Source note | uspto-grants-1996_06 |
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