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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551703Generated: October 31, 2026

Tetrahydrofuran → HCID 131728926, compound

https://huagongshe.com/reaction/551703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl DimethylphosphonoacetateHCID 4564495—
ReactantHCID 14924167HCID 14924167—
SolventWaterHCID 962—
ProductHCID 131728926HCID 131728926—

Reaction Conditions

Temperature0 °C

Reaction Steps

A tetrahydrofuran (15 mL) solution of tert-butyl dimethylphosphonoacetate (3.29 g, 14.7 mmol) was added dropwise at 0° C. over 5 minutes to a tetrahydrofuran (15 mL) suspension of sodium hydride (0.59 g, 63%, 15.5 mmol), and the mixture was stirred at 0° C. for 15 minutes. To this solution, a tetrahydrofuran (15 mL) solution of 1-methylbicyclo[3.2.0]hept-3-en-6-one (1.60 g, 13.1 mmol) was added dropwise at 0° C. over 10 minutes, and the mixture was stirred at room temperature for 4 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 (1.80 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947738B2
Source datasetuspto-grants-2011_05
ORD IDord-986e3063e52f437da94fcfbcafbf892b
Source noteuspto-grants-2011_05