HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1511368Erstellt: 24. Oktober 2026
(Trifluoromethyl)trimethylsilane → (R)-N-((S)-1-(4-bromo-2-chlorophenyl)-2,2,2-trifluoroethyl)-2-methylpropane-2-sulfinamide
https://huagongshe.com/de/reaction/1511368
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Edukt | (NZ,R)-N-[(4-bromo-2-chlorophenyl)methylidene]-2-methylpropane-2-sulfinamide | HCID 57691068 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (R)-N-((S)-1-(4-bromo-2-chlorophenyl)-2,2,2-trifluoroethyl)-2-methylpropane-2-sulfinamide | HCID 57691004 | — |
Reaktionsschritte
To a stirring solution of (R,Z)—N-(4-bromo-2-chlorobenzylidene)-2-methylpropane-2-sulfinamide (1370 mg, 4246 μmol) and (trifluoromethyl)trimethylsilane (943 μl, 6369 μmol) in DMF (5 mL) was added 1,3-bis(1-adamantyl)imidazol-2-ylidene (143 mg, 425 μmol). Reaction stirred at 35° C. for 18 h then quenched with sat NH4Cl (10 mL). Reaction partitioned between EtOAc (40 mL) and 5% NaHCO3 (10 mL). Organic dried over MgSO4, concentrated to and oil from toluene, then purified on silica (80 g) eluting with 20>30% EtOAc/Hex. Product isolated as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08212041B2 |
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| Quelldatensatz | uspto-grants-2012_07 |
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| ORD ID | ord-0e586812655441979c84f2328da396a2 |
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| Quellennotiz | uspto-grants-2012_07 |
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