HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45044Generated: October 30, 2026
Diethyl (cyanomethyl)phosphonate → 1-[(E)-2-Cyanovinyl]cyclopropanecarbonitrile
https://huagongshe.com/reaction/45044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Cyclopropanecarbonitrile, 1-formyl- | HCID 57187562 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[(E)-2-Cyanovinyl]cyclopropanecarbonitrile | HCID 57478040 | 19.2% |
Reaction Steps
To a solution of 1.0 M potassium tert-butoxide in THF (1.12 mL) at 0° C. was added slowly dropwise a solution of diethyl cyanomethylphosphonate (210 mg, 1.2 mmol) in THF (2 mL). The cold bath was removed and the reaction was warmed to ambient temperature. The solution was then re-cooled to 0° C. and a solution of 1-formylcyclopropanecarbonitrile (101 mg, 1.06 mmol) in THF (1.0 mL) was added dropwise. The cold bath was removed and the reaction was stirred for 3 hours at ambient temperature. The mixture was then diluted with ether and water, the ether solution was separated, washed with brine, dried over sodium sulfate, filtered and the solvent was removed in vacuo. Flash column chromatography (eluting with a gradient from 0-60% ethyl ether in hexanes) afforded the product (24 mg, 19%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541425B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-7ff1c7f13ff442998fd336999c2a8f1b |
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| Source note | uspto-grants-2013_09 |
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