環己烷甲酸甲酯
| 環己烷甲酸甲酯 | |
|---|---|
| 識別 | |
| CAS號 | 4630-82-4 
|
| SMILES |
|
| 性質 | |
| 化學式 | C8H14O2 |
| 摩爾質量 | 142.2 g·mol−1 |
| 外觀 | 液體 |
| 沸點 | 180 °C[1] |
| 相關物質 | |
| 相關化學品 | 3,4-環氧環己烷甲酸甲酯 |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
環己烷甲酸甲酯是一種有機化合物，化學式為C8H14O2。它可由環己烷甲酸和甲醇在硫酸存在下回流反應製得。[2]
反應[編輯]
它和正辛醇在三氟甲磺酸五氟苯銨催化下於甲苯中反應，可以得到環己烷甲酸辛酯。[4]
參考文獻[編輯]
- ^ Kirillov, N.F., Nikiforova, E.A., Vasyanin, A.N. et al. Synthesis of 16-aryl-15-oxadispiro[5.1.5.3]hexadecane-7,14-diones by reformatsky reaction. Russ J Org Chem 51, 513–517 (2015). doi:10.1134/S1070428015040089
- ^ José Maurício dos Santos Filho, Marcos Venícius Batista de Souza Castro. Synthesis, structural characterization, and antimicrobial activity of novel ferrocene-N-acyl hydrazones designed by means of molecular simplification strategy Celebrating the 100th anniversary of the birth of Professor Paulo Freire. Journal of Organometallic Chemistry. 2022. 979. 122488. doi:10.1016/j.jorganchem.2022.122488
- ^ Malek, Jaroslav. Reductions by metal alkoxyaluminum hydrides. Part II. Carboxylic acids and derivatives, nitrogen compounds, and sulfur compounds. Organic Reactions, 2004. 36. doi:10.1002/0471264180.or036.03.
- ^ Funatomi, Takashi; Wakasugi, Kazunori; Misaki, Tomonori; Tanabe, Yoo. Pentafluorophenylammonium triflate (PFPAT): An efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation. Green Chemistry, 2006. 8 (12). 1022-1027. doi:10.1039/b609181b.