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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11993생성일: 2026년 10월 24일

Ethyl cyanoacetate → 2-(2-Methylpropyl)butanedinitrile

https://huagongshe.com/ko/reaction/11993

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl cyanoacetateHCID 7764—
반응물HexaneHCID 8058—
반응물Potassium CyanideHCID 9032—
반응물3-MethylbutanalHCID 11552—
촉매PiperidineHCID 8082—
용매WaterHCID 962—
생성물2-(2-Methylpropyl)butanedinitrileHCID 1611612899%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727749B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c9764fada08d4935a6780c2b27f8914f
출처 메모uspto-grants-2010_06