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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551657Generated: November 2, 2026

Tetrahydrofuran → HCID 131728907, compound

https://huagongshe.com/reaction/551657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl DimethylphosphonoacetateHCID 4564495—
Reactant3-Cyclopentylbicyclo[3.2.0]hept-3-en-6-oneHCID 67199446—
SolventWaterHCID 962—
ProductHCID 131728907HCID 131728907—

Reaction Conditions

Temperature0 °C

Reaction Steps

A tetrahydrofuran (15 mL) solution of tert-butyl dimethylphosphonoacetate (3.21 g, 14.4 mmol) was added dropwise at 0° C. over 15 minutes to a tetrahydrofuran (15 mL) suspension of sodium hydride (0.59 g, 63%, 15.7 mmol), and the mixture was stirred at 0° C. for 25 minutes. To this solution, a tetrahydrofuran (15 mL) solution of 3-cyclopentylbicyclo[3.2.0]hept-3-en-6-one (2.30 g, 13.1 mmol) was added dropwise at 0° C. over 10 minutes, and the mixture was stirred at room temperature for 16 hours. The mixture was treated with water, followed by extraction with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography to obtain the compound of interest as a yellow oil substance (3.30 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947738B2
Source datasetuspto-grants-2011_05
ORD IDord-0a684cbeff404465a59c378ee8c9bccb
Source noteuspto-grants-2011_05