HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397504Generated: October 30, 2026
Ethyl cyanoacetate → Ethyl 2-cyano-2-cyclopentylideneacetate
https://huagongshe.com/reaction/1397504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-cyano-2-cyclopentylideneacetate | HCID 223257 | — |
Reaction Steps
To an ambient solution of hexamethyldisilazane (17.7 mL, 84.0 mmol) in acetic acid (56 mL) was added sequentially cyclopentanone (5.0 mL, 56.3 mmol) and ethyl 2-cyanoacetate (12.0 mL, 113 mmol). The solution was heated to 70° C. for 15 hours. The reaction was cooled to room temperature and diluted with water (100 mL) and ethyl acetate (100 mL). The layers were separated, and the aqueous was extracted with additional ethyl acetate (2×100 mL). The combined organics were dried with anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by chromatography on SiO2 gel, eluting with 100% hexane to 5% ethyl acetate in hexane, to give the title product as a white, solid. MS (ESI) m/z 180 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901152B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-60c1d91605664d369f9d83c0bc6b1aeb |
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| Source note | uspto-grants-2014_12 |
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