Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346849Erstellt: 25. Oktober 2026

Styrene Oxide → 2-[2-Methyl-5-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-2,3-dihydro-indol-1-yl]-2-phenyl-ethanol

https://huagongshe.com/reaction/346849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktStyrene OxideHCID 7276—
EduktAmmonium ChlorideHCID 25517—
Edukt2-methyl-5-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-2,3-dihydro-1H-indoleHCID 21082212—
EduktLithium perchlorateHCID 23665649—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-[2-Methyl-5-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-2,3-dihydro-indol-1-yl]-2-phenyl-ethanolHCID 2108220752,5%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 114 mg (0.275 mmol) of 2-methyl-5-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-2,3-dihydro-1H-indole (example 51.2) in 1 mL of acetonitrile were added 0.063 mL (0.55 mmol) of racemic phenyloxirane and 58 mg (55 mmol) of lithiumperchlorate. After stirring at 80° C. for 18 hrs, the mixture was distributed between Et2O and a saturated aqueous solution of NH4Cl. The combined organic phases were dried over Na2SO4 and evaporated. Column chromatography on silica gel with n-heptane/EtOAc 4:1 yielded 77 mg (52%) of 2-[2-methyl-5-(2,2,2-trifluoro-1-triethylsilanyloxy-1-trifluoromethyl-ethyl)-2,3-dihydro-indol-1-yl]-2-phenyl-ethanol, MS: 534 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173048B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-39c5ce7bf222446787f9bac80aaaa14d
Quellennotizuspto-grants-2007_02