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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654961Generated: November 1, 2026

Acetic Anhydride → 4-[1-Acetoxy-2-[3-(2-naphthyl)propoxy]ethyl]-2-trimethylsilylfuran

https://huagongshe.com/reaction/654961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant5-(Trimethylsilyl)furan-3-carbaldehydeHCID 15663251—
Reactant(2-Naphthyl)propyl tributylstannylmethyl etherHCID 67916977—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-[1-Acetoxy-2-[3-(2-naphthyl)propoxy]ethyl]-2-trimethylsilylfuranHCID 19885955—

Reaction Steps

n-Butyl lithium (a 1.6M solution in hexane; 0.69 ml, 1.1 mmol) was added dropwise to a solution of (2-naphthyl)propyl tributylstannylmethyl ether (511.9 mg, 1.05 mmol) in tetrahydrofuran (5 ml) at -78° under argon. After 5 minutes, a solution of 5-trimethylsilyl-3-furaldehyde (176 mg, 1.05 mmol) in tetrahydrofuran (1/2 ml) was added, followed by acetic anhydride (0.1 ml, 1.58 mmol) after 25 minutes. Stirring was continued at -78° for 1 hour and the mixture was quenched with water. Extraction (ethyl ether) and evaporation of the dried (magnesium sulphate) extracts gave an oil, which was flash chromatographed using 10% ethyl ether/petroleum ether. The title ester was obtained as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05134128
Source datasetuspto-grants-1992_07
ORD IDord-74cd7567e79744d8857324b441807050
Source noteuspto-grants-1992_07