Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 470010Erstellt: 25. Oktober 2026

Triphenylphosphine → N-[3-(3-methyl-but-3-enyloxy)-phenyl]-acetamide

https://huagongshe.com/reaction/470010

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt3-HydroxyacetanilideHCID 12124—
Edukt3-Methyl-3-buten-1-olHCID 12988—
EduktDiethyl azodicarboxylateHCID 5462977—
EduktAcetic acid 3-formylamino-phenyl esterHCID 57470213—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
ProduktN-[3-(3-methyl-but-3-enyloxy)-phenyl]-acetamideHCID 5756738452%

Reaktionsschritte

A suspension of the mixture of N-(3-hydroxy-phenyl)-acetamide and acetic acid 3-formylamino-phenyl ester (18.12 g, 0.12 mol), 3-methyl-but-3-en-1-ol (8.6 g, 0.1 mol), DEAD (87 g, 0.2 mol) and Ph3P (31.44 g, 0.12 mol) in benzene (250 mL) was heated at reflux overnight and then cooled to room temperature. The reaction mixture was poured into water and the organic layer was separated. The aqueous phase was extracted with EtOAc (300×3 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and concentrated. The residue was purified by column chromatography to give N-[3-(3-methyl-but-3-enyloxy)-phenyl]-acetamide (11 g, 52%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629162B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-a4af9d3a0f5b4404b7110f44889c9b87
Quellennotizuspto-grants-2014_01