丁炔二酸二乙酯

化合物

丁炔二酸二乙酯是一種不飽和羧酸酯,化學式為C8H10O4,它可由丁炔二酸乙醇硫酸催化下反應得到。[3]它在鎳鈀合金催化下加氫,可以得到丁二酸二乙酯[4]它和其它炔烴一樣,可以發生聚合反應,它自身三聚得到苯六甲酸六乙酯。[5]

丁炔二酸二乙酯
識別
CAS號 762-21-0  checkY
性質
化學式 C8H10O4
摩爾質量 170.16 g·mol−1
熔點 1.5 °C[1]
沸點 108~118 °C(10 torr)[2]
相關物質
相關化學品 丁炔二酸
丁炔二酸二甲酯
馬來酸二乙酯
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

參考文獻

  1. ^ "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2021-09-20].
  2. ^ J. F. Grove. The Fungistatic Activity of Ethylenic and Acetylenic Compounds.: Esters of Halogenofumaric Acids and Acetylene Dicarboxylic Acid. Annals of Applied Biology. 1948-03, 35 (1): 37–44 [2021-09-20]. ISSN 0003-4746. doi:10.1111/j.1744-7348.1948.tb07348.x (英語). 
  3. ^ William E. Truce, Robert B. Kruse. The Stereochemistry of the Base-catalyzed Addition of p-Toluenethiol to Disodium and Diethyl Acetylenedicarboxylate 1,2. Journal of the American Chemical Society. 1959-10, 81 (20): 5372–5374 [2021-09-20]. ISSN 0002-7863. doi:10.1021/ja01529a030 (英語). 
  4. ^ Yasin Çetinkaya, Önder Metin, Metin Balci. Reduced graphene oxide supported nickel–palladium alloy nanoparticles as a superior catalyst for the hydrogenation of alkenes and alkynes under ambient conditions. RSC Advances. 2016, 6 (34): 28538–28542 [2021-09-20]. ISSN 2046-2069. doi:10.1039/C5RA25376D (英語). 
  5. ^ Nicolas Agenet, Olivier Buisine, Franck Slowinski, Vincent Gandon, Corinne Aubert, Max Malacria. John Wiley & Sons, Inc. , 編. Cotrimerizations of Acetylenic Compounds. Hoboken, NJ, USA: John Wiley & Sons, Inc. 2007-03-12: 1–302 [2021-09-20]. ISBN 9780471264187. doi:10.1002/0471264180.or068.01. (原始內容存檔於2022-03-08) (英語).