HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876880Generated: November 1, 2026
Diethyl (cyanomethyl)phosphonate → HCID 66824380, compound
https://huagongshe.com/reaction/1876880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| Reactant | 3-Oxocyclobutane-1-carbonitrile | HCID 13082390 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66824380 | HCID 66824380 | 23.3% |
Reaction Steps
To a solution of 1.0 M of potassium tert-butoxide in tetrahydrofuran (78.4 mL) at 0° C. was added drop wise a solution of diethyl cyanomethylphosphonate (13.3 mL, 0.0822 mol) in tetrahydrofuran (100 mL, 2 mol). The reaction was warmed to room temperature and then cooled at 0° C. again. To the reaction mixture was a solution of 3-oxocyclobutanecarbonitrile (7.10 g, 0.0746 mol) in tetrahydrofuran (70 mL). The reaction was allowed to warm up to room temperature and stirred overnight. After being quenched with water, the mixture was extracted with ether. The combined organic layers were washed with water, brine, dried over MgSO4, and evaporated to dryness. The crude mixture was purified on silica gel, eluting with 0 to 40% EtOAc in hexanes, to give the desired product (2.05 g, 23.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309718B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-05e17778aef3428a9bc002871ea9cd72 |
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| Source note | uspto-grants-2012_11 |
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