Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1681532Erstellt: 27. Oktober 2026

Acetic Anhydride → 3(-1-Acetoxytridecyl)-4-phenylfuran

https://huagongshe.com/reaction/1681532

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt4-Phenyl-3-furaldehydeHCID 15037148—
EduktHCID 178443215HCID 178443215—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3(-1-Acetoxytridecyl)-4-phenylfuranHCID 15037156—

Reaktionsschritte

Dodecylmagnesium bromide (a 1.0M solution in THF; 2.11 ml, 2.11 mmol) was added to a solution of 4-phenyl-3-furaldehyde (303 mg, 1.76 mmol) in THF at 0 degrees under argon and gradually allowed to warm to room temperature with stirring. When all of the aldehyde was consumed acetic anhydride (719 mg, 7.04 mmol) was added and stirring was continued for 2 hours more. The reaction was quenched with saturated ammonium chloride and the organics were extracted into ethyl ether. The combined fractions were washed with saturated sodium bicarbonate, water and brine, dried over magnesium sulfate and concentrated to a yellow oil which was purified by flash chromatography on silica using 3% ethyl ether hexanes to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05171863
Quelldatensatzuspto-grants-1992_12
ORD IDord-c6e642d6473f49f289fd4c4ab8dc3d5e
Quellennotizuspto-grants-1992_12