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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551635Generated: November 2, 2026

Tetrahydrofuran → HCID 131728897, compound

https://huagongshe.com/reaction/551635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl DimethylphosphonoacetateHCID 4564495—
ReactantHCID 67198837HCID 67198837—
SolventWaterHCID 962—
ProductHCID 131728897HCID 131728897—

Reaction Conditions

Temperature0 °C

Reaction Steps

A tetrahydrofuran (15 mL) solution of tert-butyl dimethylphosphonoacetate (3.70 g, 16.5 mmol) was added dropwise at 0° C. over 20 minutes to a tetrahydrofuran (15 mL) suspension of sodium hydride (0.68 g, 63%, 18.0 mmol), and the mixture was stirred at 0° C. for 20 minutes. To this solution, a tetrahydrofuran (15 mL) solution of (±)-(1S,5R)-3-isopropylbicyclo[3.2.0]hept-3-en-6-one (2.25 g, 15.0 mmol) was added dropwise at 0° C. over 15 minutes, and the mixture was stirred at room temperature for 2 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 (3.00 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947738B2
Source datasetuspto-grants-2011_05
ORD IDord-66a95e28f44b427898e266eddf553d5c
Source noteuspto-grants-2011_05