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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551700Generated: November 1, 2026

Tetrahydrofuran → HCID 86646158, compound

https://huagongshe.com/reaction/551700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantTrimethyl phosphonoacetateHCID 80029—
Reactant6-Hepten-3-oneHCID 137641—
SolventWaterHCID 962—
ProductHCID 86646158HCID 86646158—

Reaction Conditions

Temperature0 °C

Reaction Steps

A tetrahydrofuran (25 mL) solution of trimethyl phosphonoacetate (4.67 g, 25.1 mmol) was added dropwise at 0° C. over 1 hour to a tetrahydrofuran (25 mL) suspension of sodium hydride (1.04 g, 63%, 27.4 mmol). To the mixture, tetrahydrofuran (25 mL) was further added, and the mixture was then stirred at 0° C. for 1 hour. To this solution, a tetrahydrofuran (25 mL) solution of 6-hepten-3-one (2.56 g, 22.8 mmol) was added dropwise at 0° C. over 20 minutes, and the mixture was stirred at room temperature for 2.5 hours and subsequently stirred at 65° C. for 3 hours. The mixture was treated with water, and volatile portions were then distilled off under reduced pressure, followed by extraction with hexane. The organic layer was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure to obtain the compound of interest as a pale yellow oil substance (3.04 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947738B2
Source datasetuspto-grants-2011_05
ORD IDord-5060a565fd4f4bffa67678f38a41f09c
Source noteuspto-grants-2011_05