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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 450210Erstellt: 23. Oktober 2026

Imidazole → 3-(tert-Butyl-dimethyl-silanyloxymethyl)-5-trifluoromethyl-phenylamine

https://huagongshe.com/de/reaction/450210

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktSodium FluorideHCID 5235—
EduktEthyl AcetateHCID 8857—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
Edukt3-Amino-5-(trifluoromethyl)benzoic acidHCID 609556—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(tert-Butyl-dimethyl-silanyloxymethyl)-5-trifluoromethyl-phenylamineHCID 137329775—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 3-Amino-5-trifluoromethyl-benzoic acid (2.0 g, 9.76 mmol) in THF (40 mL) at 0° C. is added LiAlH4 in THF (1 M, 39 mL). The mixture is warmed to reflux and stirred for 62 h. The mixture is then cooled to 0° C. and NaF (2.2 g) is added followed by H2O (3.8 mL). The slurry is stirred for 10 minutes and then allowed to warm to rt and stir an additional 40 min. The mixture is filtered and the solid is rinsed with EtOAc and MeOH. The filtrate is concentrated and the crude residue is mixed with imidazole (2.66 g, 39 mmol) and DCM (30 mL) at 0° C. TBSCl (3.5 g, 23.4 mmol) is added and the mixture is stirred at rt for 5 h. The reaction mixture is then diluted with EtOAc, washed with saturated aqueous NaHCO3, brine, and dried over Na2SO4. Concentration provides the title compound that is carried on to next step without further purification. MS (ESI) m/z 306.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08486954B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-4aad8827560d4276b4d0395a1dac412c
Quellennotizuspto-grants-2013_07