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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413212Generated: November 2, 2026

Tetrahydrofuran → HCID 54549583, compound

https://huagongshe.com/reaction/413212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAcetic acid, anhydride with diethyl hydrogen phosphateHCID 18353—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl 5-formylthiophene-2-carboxylateHCID 21473735—
ProductHCID 54549583HCID 54549583—

Reaction Conditions

Temperature60 °C

Reaction Steps

1.7 g (8 mmol) of the product obtained in step c) were dissolved in 5 ml of dry tetrahydrofuran. The solution was added dropwise to a mixture of 2.24 g (10 mmol) of diethyl phosphonoacetate and 440 mg sodium hydride (55% in paraffin oil) in 30 ml of dry tetrahydrofuran. The resulting mixture was stirred at 60° C. for 3 hours. After cooling to room temperature, the mixture was poured onto water/ethyl acetate. The organic phase was separated, washed with 10% aqueous citric acid and dried with anhydrous magnesium sulfate. After filtration, the solvents were removed to give 2.6 g of raw product. This material was purified by column chromatography (silica gel; ethyl acetate/n-heptane (1/5; v/v)). The fractions containing the title compound were combined and evaporated to give 1.2 g of a clear light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566366B1
Source datasetuspto-grants-2003_05
ORD IDord-26fe0739877241a9bac63d42659a1686
Source noteuspto-grants-2003_05