Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 577622Erstellt: 25. Oktober 2026

1,4-Dimethoxy-2-butyne → 2-(Trifluoroacetylamino)-5,6-bis(methoxymethyl)indane

https://huagongshe.com/reaction/577622

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-Dimethoxy-2-butyneHCID 542354—
Edukt2,2,2-trifluoro-N-[1-(2-propynyl)-3-butynyl]acetamideHCID 22499180—
KatalysatorChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
LösungsmittelEthanolHCID 702—
Produkt2-(Trifluoroacetylamino)-5,6-bis(methoxymethyl)indaneHCID 22499220—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

According to the procedure of Magnus et. al (Tetrahed. Lett., 34, 23-26 (1993)) a solution of commercially available 1,4-dimethoxy-2-butyne (1.32 g, 11.5 mmol) in nitrogen-degassed ethanol is heated to 80° C. with stirring under a nitrogen atmosphere. Tris(triphenylphosphine)rhodium chloride (64 mg, 0.07 mmol) and a solution of 2,2,2-trifluoro-N-[1-(2-propynyl)-3-butynyl]-acetamide (470 mg, 2.32 mmol; prepared from literature procedure; Romero, Arthur G.; Leiby, Jeffrey A PCT Int. Appl. WO 9623760) in nitrogen-degassed ethanol (2 ml) are added in portions over 2 hours. The mixture is stirred under nitrogen at 80° C. for a further 3 hours. The solvent is removed under vacuo and the residue is purified by flash chromatography on silica gel, elating with hexane/ethyl acetate (2:1)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040559B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-2950db03f6884be6866aabd44cd0ab06
Quellennotizuspto-grants-2015_05