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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37224Erstellt: 24. Oktober 2026

Potassium Iodide → Methyl 2-(4-Tert-Butyldimethylsilyloxymethyl-2-Allylphenoxy)-2-Phenylacetate

https://huagongshe.com/de/reaction/37224

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
Edukt18-Crown-6HCID 28557—
EduktMethyl 2-(2-bromophenyl)acetateHCID 8063364—
Edukt4-Tert-butyldimethylsilyloxymethyl-2-allylphenolHCID 19934838—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 2-(4-Tert-Butyldimethylsilyloxymethyl-2-Allylphenoxy)-2-PhenylacetateHCID 1993485165,4%

Reaktionsschritte

To a suspension of KH (1.3 eq) in DMF (1 mL) was added a solution of the product of Step C (157 mg, 0.566 mmol) in DMF (1 mL), followed by 18-crown-6 (30 mg; 0.2 eq). The reaction mixture was stirred for 5 minutes at room temperature. A solution of methyl 2-bromophenylacetate (168 mg, 0.735 mmol) in DMF (1 mL) was added, followed by a catalytic amount of potassium iodide. The reaction was heated to 80° C. for 0.5 hours then stirred at room temperature for 16 hours. After concentration in vacuo, the residue was partitioned between water and ethyl acetate. The combined organic layers were washed with water, brine, then dried (MgSO4). After filtration and concentration in vacuo, the residue was chromatographed on silica (MPLC, ethyl acetate/hexanes (5/95)) to afford 158 mg (66%) of the title compound (Rf =0.22, 5% ethyl acetate/hexanes).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420133
Quelldatensatzuspto-grants-1995_05
ORD IDord-c0cc3718b5c04f88bf7fffa683d15765
Quellennotizuspto-grants-1995_05