Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488242Generated: October 25, 2026

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

https://huagongshe.com/reaction/488242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Phenyl-3-furaldehydeHCID 15037148—
ReactantHCID 178443215HCID 178443215—
SolventTetrahydrofuranHCID 8028—
Product3(-1-Acetoxytridecyl)-4-phenylfuranHCID 15037156—

Reaction Steps

Dodecylmagnesium bromide (a 1.0 M 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298633
Source datasetuspto-grants-1994_03
ORD IDord-5809f04bcb0a429c8934fe1bd1b551a3
Source noteuspto-grants-1994_03