Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (Chloromethyl)dimethylisopropoxysilane | HCID 266137 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 69943808 | HCID 69943808 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69944199 | HCID 69944199 | — |
| Product | HCID 178460657 | HCID 178460657 | — |
Reaction Steps
(Dimethylisopropoxysilyl)methylmagnesium chloride was prepared from a solution of 5.74 g (34.4 mmol) of chloromethyldimethylisopropoxysilane in 40 ml tetrahydrofuran and 0.84 g (34.4 mmol) of metallic magnesium. A solution of 4.65 g (17.2 mmol) of (2R)-2′,3′-difluoro-2-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)propiophenone [prepared as described in Step 7(i) above] in 20 ml of tetrahydrofuran was added to the solution of the Grignard reagent at 0° C. with stirring. The resulting mixture was stirred at ambient temperature for 30 minutes, after which the reaction was stopped by the addition of a saturated aqueous ammonium chloride solution to the reaction mixture. The reaction product was extracted with ethyl acetate. The organic layer was washed with aqueous sodium chloride solution and concentrated to afford 8.1 g of crude (2S,3R)-2-(2,3-difluorophenyl)-1-(isopropoxydimethylsilyl)-3-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)-2-butanol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06392082B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-5fa380011da44907994c362274a60505 |
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| Source note | uspto-grants-2002_05 |
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