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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278480Erstellt: 25. Oktober 2026

Imidazole → Methyl 3-[4-(tert-butyldimethylsilyloxy)-3-oxobutyl]phenylacetate

https://huagongshe.com/reaction/278480

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
Edukttert-Butyldimethylsilyl chlorideHCID 28928—
EduktMethyl 3-(4-hydroxy-3-oxobutyl)phenylacetateHCID 22628477—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 3-[4-(tert-butyldimethylsilyloxy)-3-oxobutyl]phenylacetateHCID 2262845994,9%

Reaktionsschritte

To an ice cooled solution of methyl 3-(4-hydroxy-3-oxo-butyl)phenylacetate (472 mg, 2.00 mmol) in DMF (10 ml) was added imidazole (264 mg, 3.88 mmol) followed by tert-butyldimethylsilyl chloride (408 mg, 5.99 mmol). After 30 minutes the ice-bath was removed and then the mixture was stirred overnight at room temperature. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate. The organic layer was washed with brine, dried (magnesium sulfate), and concentrated in vacuo. The residue was purified by silica gel (20 g) column chromatography eluting with hexane/ethyl acetate (10:1) to give methyl 3-[4-(tert-butyldimethylsilyloxy)-3-oxobutyl]phenylacetate (664 mg, 94.9%) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06359145B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-b774a9a2e1924066b5eae6f3b0d8fa73
Quellennotizuspto-grants-2002_03