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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 864492Erstellt: 26. Oktober 2026

Diethyl Ether → 1,1-Diphenylacetone

https://huagongshe.com/reaction/864492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
Edukt2,2-Diphenylacetyl chlorideHCID 74637—
EduktPotassium FluorideHCID 522689—
EduktTri-n-butyl-((3,5-bis(trifluoromethyl)phenyl)methyloxymethyl)tinHCID 85682165—
LösungsmittelChloroformHCID 6212—
Produkt1,1-DiphenylacetoneHCID 69907—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Diphenylacetyl chloride (4.6 g), tri-n-butyl-((3,5-bis(trifluoromethyl)phenyl)methyloxymethyl)tin (12.6 g; Example 1a, (Method Ai)and benzylchlorobis(triphenylphosphine) palladium (II)(80 mg)were dissolved in chloroform (10 ml) and the solution heated at 80° C. for 6h. On cooling diethyl ether and saturated aqueous potassium fluoride were added and after 30 minutes the solution was filtered through Hiflo™. The organic layer was washed with water, saturated brine and dried (MgSO4). After evaporation in vacuo the residual oil was purified by chromatography on silica gel (eluting with 0 to 10% ethyl acetate in petroleum ether bp=60°-80° C.) to give 1-(3,5-bis(trifluoromethyl)phenyl)methyloxy)-3,3-diphenyl acetone as an oil. 1H NMR (CDCl3, 360MHz) δ7.80 (1H; s; 4-aryl CH) 7.71 (2H; s; 2,6-aryl CH), 7.43-7.24 (10H; m; phenyl), 5.30 (1H; s; Ph2CH), 4.56 (2H; s), 4.31 (2H; s). m/e Found 452.1191, C24H13F6O2 requires 452.12110.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05563161
Quelldatensatzuspto-grants-1996_10
ORD IDord-cfa0d90d320c4607a1d2e6bcdc8c5fd8
Quellennotizuspto-grants-1996_10