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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2246651Erstellt: 27. Oktober 2026

Ethyl trimethylsilylacetate → Ethyl 3-(4-(benzyloxy)phenyl)-3-(3-methyl-3H-1,2,3-triazol-4-yl)acrylate

https://huagongshe.com/reaction/2246651

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl trimethylsilylacetateHCID 77687—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt(4-(Benzyloxy)phenyl)(3-methyl-3H-1,2,3-triazol-4-yl)methanoneHCID 57835886—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 3-(4-(benzyloxy)phenyl)-3-(3-methyl-3H-1,2,3-triazol-4-yl)acrylateHCID 6868752895,2%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of lithium bis(trimethylsilyl)amide (22 mmol, 1 m in THF) was added ethyl trimethylsilylacetate (31.5 mmol) dropwise at −78° C. After 20 minutes at −78° C., a solution of 3.3 (14.7 mmol) in THF (50 mL) was added dropwise, and the reaction was maintained at −78° C. for 4 hours. The reaction was quenched with saturated NH4Cl (aq) and warmed to room temperature. The mixture was extracted with EtOAc (500 mL), dried over anhydrous sodium sulfate, filtered, and concentrated with silica gel under reduced pressure. The residue was chromatographed (silica gel, 1:1 EtOAc/hexane) to afford compound 3.4 (5.1 g, 14 mmol). MS ESI (pos.) m/e 364.1 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07687526B2
Quelldatensatzuspto-grants-2010_03
ORD IDord-3e831d8f3add4d1892ca29abc66b938c
Quellennotizuspto-grants-2010_03