HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551700Generated: November 1, 2026
Tetrahydrofuran → HCID 86646158, compound
https://huagongshe.com/reaction/551700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Trimethyl phosphonoacetate | HCID 80029 | — |
| Reactant | 6-Hepten-3-one | HCID 137641 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86646158 | HCID 86646158 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947738B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-5060a565fd4f4bffa67678f38a41f09c |
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| Source note | uspto-grants-2011_05 |
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