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HRID 16329Erstellt: 24. Oktober 2026
Imidazole → tert-butyl [(1R,2R)-2-(tert-butyldiphenylsilanyloxy)-1-(3,4,5-trifluorophenyl)propyl]carbamate
https://huagongshe.com/de/reaction/16329
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Imidazole | HCID 795 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Edukt | tert-butyl [(1R,2R)-2-hydroxy-1-(3,4,5-trifluorophenyl)propyl]carbamate | HCID 68717986 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | tert-butyl [(1R,2R)-2-(tert-butyldiphenylsilanyloxy)-1-(3,4,5-trifluorophenyl)propyl]carbamate | HCID 68718850 | — |
Reaktionsschritte
In nitrogen atmosphere, tert-butyldiphenylsilyl chloride (2.0 mL) was added dividedly four times to a DMF solution (3 mL) of [(1R,2R)-2-hydroxy-1-(3,4,5-trifluorophenyl)propyl]-carbamic acid tert-butyl ester (610 mg) and imidazole (817 mg). This reaction solution was stirred at room temperature for 3 hr. To the reaction solution, ethyl acetate and water were added. The organic layer was separated, washed with 1 N hydrochloric acid, water, a saturated sodium hydrogencarbonate aqueous solution, and saturated saline in this order. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: hexane:diethylether=49:1 to 19:1) to give 684 mg of the title compound. The physical property values of this compound were as follows:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737141B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-cbe249a5d1264e269f037a95cd7c9cbc |
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| Quellennotiz | uspto-grants-2010_06 |
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