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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681532Generated: October 26, 2026

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

https://huagongshe.com/reaction/1681532

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 1.0M 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05171863
Source datasetuspto-grants-1992_12
ORD IDord-c6e642d6473f49f289fd4c4ab8dc3d5e
Source noteuspto-grants-1992_12