Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 59586724 | HCID 59586724 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59586696 | HCID 59586696 | — |
Reaction Steps
A solution of 355 mg (0.47 mmol) of the product from example 70A in 9 ml of THF is admixed with 290 mg (1.10 mmol) of a 1 molar solution of tetrabutylammonium fluoride in THF. The mixture is stirred at RT for 2 h. Then it is admixed with 80 ml of water, 50 ml of ethyl acetate and 6 ml of sodium chloride solution, and the phases are separated. The organic phase is extracted twice with ethyl acetate and the combined organic phases are dried over sodium sulfate. After filtration, the mixture is freed of the solvent and the residue is prepurified by chromatography on silica gel (20:1 dichloromethane/methanol). Subsequent purification by means of preparative HPLC with an acetonitrile/water mixture affords 39 mg (16% of theory) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198267B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-2c509b7c7e6b49e6bbc1e3973c03acde |
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| Source note | uspto-grants-2012_06 |
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