HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053549Generated: October 29, 2026
tert-Butyl Dimethylphosphonoacetate → HCID 131736285, compound
https://huagongshe.com/reaction/1053549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl Dimethylphosphonoacetate | HCID 4564495 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 71582576 | HCID 71582576 | — |
| Catalyst | tert-Butyl Dimethylphosphonoacetate | HCID 4564495 | — |
| Catalyst | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131736285 | HCID 131736285 | 134.2% |
Reaction Steps
Potassium t-butoxide (8.66 g) was dissolved in tetrahydrofuran (50 mL) under a nitrogen atmosphere, and the solution was then cooled to approximately 5° C. Tert-butyl (dimethoxyphosphoryl)acetate (17.30 g) was added thereto at 15° C. or lower, and the mixture was stirred at 5 to 15° C. for 1 hour. (1R,5S)-3-Ethylbicyclo[3.2.0]hept-3-en-6-one (10.00 g) and tetrahydrofuran (25 mL) were further added thereto, and the mixture was stirred at 5 to 15° C. for 1.5 hours. Potassium t-butoxide (0.90 g) and tert-butyl(dimethoxyphosphoryl)acetate (1.73 g) were further added thereto, and the mixture was stirred for approximately 1 hour. Then, the reaction mixture was separated into aqueous and organic layers by the addition of toluene (85 mL) and water (40 mL). The organic layer was washed twice with water (20 mL) and then concentrated under reduced pressure to obtain tert-butyl [(1R,5S)-3-ethylbicyclo[3.2.0]hept-3-en-6-ylidene]acetate (23.09 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394235B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-7c386574e7a9482faa7bc59c4ac68082 |
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| Source note | uspto-grants-2016_07 |
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