HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11993Generated: October 26, 2026
Ethyl cyanoacetate → 2-(2-Methylpropyl)butanedinitrile
https://huagongshe.com/reaction/11993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 3-Methylbutanal | HCID 11552 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Methylpropyl)butanedinitrile | HCID 16116128 | 99% |
Reaction Steps
A mixture of ethyl cyanoacetate (73.3 g, 6.48 mol), isovaleraldehyde (613.9 g, 7.13 mol), piperidine (5.5 g, 0.065 mol), and hexane (0.5 L) was placed under reflux with continuous removal of water. When no additional water was collected, the mixture was cooled and distilled under vacuum to remove solvent. Isopropanol (1 L) was added to the remaining oil, followed by a solution of potassium cyanide (422 g, 6.48 mol) in water (2 L). The reaction mixture was maintained below 35° C. during addition of the potassium cyanide solution and then held at approximately 35° C. for 4 h. The reaction mixture was distilled at atmospheric pressure until a temperature of 95° C. was reached and then refluxed at this temperature for 5 h. The reaction mixture was cooled, diluted with water (0.5 L) and extracted with 1 L methyl tert-butyl ether (MTBE). The MTBE extract was washed with water (0.5 L), dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum to give 873.4 g of 2-isobutyl-succinonitrile as an oil. Purified samples of 2-isobutyl-succinonitrile can be obtained by vacuum distillation (90° C. at 0.275 mm Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07727749B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-c9764fada08d4935a6780c2b27f8914f |
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| Source note | uspto-grants-2010_06 |
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