Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Product | HCID 66962058 | HCID 66962058 | — |
Reaction Steps
A 1 M tetrahydrofuran solution of tetrabutylammonium fluoride (6.44 ml, 6.44 mmol) was added to a solution of 2.13 g (5.85 mmol) of the title compound in step (v) of Example XA1 in diethyl ether (5 ml), and the mixture was stirred at room temperature for 10 min. Tetrahydrofuran (5 ml) was added to the reaction solution, and the mixture was stirred at room temperature for 2 hr. An aqueous ammonium chloride solution was added thereto, and the mixture was extracted with diethyl ether. The organic layer was washed with brine, was dried over anhydrous sodium sulfate and was then filtered. The filtrate was concentrated at a low temperature under the reduced pressure, and the residue was purified by distillation to give 545.4 mg (yield 74%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879808B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-d31896f1358d4e92aa14bc23c5fb31cd |
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| Source note | uspto-grants-2011_02 |
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