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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2075055Erstellt: 27. Oktober 2026

Water → (2-(Cyclohexyl(methoxy)methyl)-5-(trifluoromethyl)phenyl)methanol

https://huagongshe.com/reaction/2075055

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTetrabutylammonium FluorideHCID 2724141—
Edukt(2-(Cyclohexyl(methoxy)methyl)-5-(trifluoromethyl)benzyloxy)(tert-butyl)dimethylsilaneHCID 58968692—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2-(Cyclohexyl(methoxy)methyl)-5-(trifluoromethyl)phenyl)methanolHCID 5896873488%

Reaktionsschritte

To a solution of (2-(cyclohexyl(methoxy)methyl)-5-(trifluoromethyl)benzyloxy)(tert-butyl)dimethylsilane (1.13 g, 2.4 mmol) in THF (5 mL) at room temperature was added TBAF in THF (1.0 M, 4.8 mL, 4.8 mmol). The mixture was stirred at room temperature overnight. Water was added and the mixture was extracted with ethyl acetate. Combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo. The residue was purified by chromatography over 25+M Biotage silica column (eluted with 0-30% ethyl acetate in heptane) to afford the title compound (633.9 mg, 88%). 1H NMR (400 MHz, CDCl3) δ ppm 0.91-1.27 (m, 6H) 1.63-1.70 (m, 3H) 1.72-1.81 (m, 1H) 2.07 (d, J=12.86 Hz, 1H) 2.33-2.42 (m, 1H) 3.18 (s, 3H) 4.10 (d, J=7.88 Hz, 1H) 4.78 (dd, J=5.81, 3.32 Hz, 2H) 7.43 (d, J=7.88 Hz, 1H) 7.55 (d, J=8.30 Hz, 1H) 7.69 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07919506B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-5fafb6bc74174aba9782d556b7a48049
Quellennotizuspto-grants-2011_04