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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089856Generated: November 1, 2026

Ethyl Acetate → 2-[(2-Methoxyfluoren-9-yl)ethyl]-1,3-dioxolane

https://huagongshe.com/reaction/1089856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-MethoxyfluoreneHCID 17301—
Reactant2-(2-Bromoethyl)-1,3-dioxolaneHCID 87776—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-[(2-Methoxyfluoren-9-yl)ethyl]-1,3-dioxolaneHCID 5386645668.3%

Reaction Steps

A solution of n-BuLi (2.5 M in hexane, 6.4 mL, 16.0 mmol) was slowly added into a cooled (-78° C.) solution of 2-methoxyfluorene (prepared according to example 10; 3.1 g, 15.8 mmol) in 100 ml THF. The reaction mixture became dark red and a solid started to precipitate out. After 30 minutes 2-(2-bromoethyl)-1,3-dioxolane (5.8 g, 32.0 mmol) was added to the cold solution and the solution was warmed up to room temperature. The reaction mixture was stirred overnight at room temperature. TLC (silica, 25% EtOAc in hexane) was used to monitor the reaction. The reaction was quenched with water and the product was extracted into EtOAc. The organic layer was washed with water (×3), dried over magnesium sulfate and evaporated. Short path chromatography (5% ethyl acetate/hexane) afforded 3.2 g (62.5%) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079260
Source datasetuspto-grants-1992_01
ORD IDord-e88bbb653ace4aaea305f0e3d8cb53ff
Source noteuspto-grants-1992_01