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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 865527Erstellt: 25. Oktober 2026

Triethylamine → Methyl alpha-(4-tert-butyldimethylsilyloxy-methyl-2-n-propylphenoxy)-3,4-methylenedioxyphenylacetate

https://huagongshe.com/reaction/865527

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl AcetateHCID 8857—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
EduktMethyl alpha-(4-hydroxymethyl-2-n-propyl-phenoxy)-3,4-methylenedioxyphenylacetateHCID 19080423—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl alpha-(4-tert-butyldimethylsilyloxy-methyl-2-n-propylphenoxy)-3,4-methylenedioxyphenylacetateHCID 13171961797%

Reaktionsschritte

To a solution of 2.50 g (6.98 mmol) of the product of Step A dissolved in 20 mL of dichloromethane was added 1.95 mL (14.0 mmol) of triethylamine, 1.26 g (8.38 mmol) of tert-butyldimethylchlorosilane, 85 mg (0.1 eq) of 4-dimethylaminopyridine and the reaction mixture was stirred at room temperature for 30 minutes under a nitrogen atmosphere. The reaction was then diluted with 100 mL EtOAc, washed with water, 1.0 N HCl, saturated aqueous NaHCO3, saturated NaCl, dried (MgSO4), filtered and evaporated in vacuo to afford 3.20 g (97%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05565485
Quelldatensatzuspto-grants-1996_10
ORD IDord-97234efc43434420864aea725558d053
Quellennotizuspto-grants-1996_10