HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551657Generated: November 2, 2026
Tetrahydrofuran → HCID 131728907, compound
https://huagongshe.com/reaction/551657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl Dimethylphosphonoacetate | HCID 4564495 | — |
| Reactant | 3-Cyclopentylbicyclo[3.2.0]hept-3-en-6-one | HCID 67199446 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131728907 | HCID 131728907 | — |
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
| 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-0a684cbeff404465a59c378ee8c9bccb |
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| Source note | uspto-grants-2011_05 |
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