對甲苯磺酸肉桂酯
對甲苯磺酸肉桂酯 | |
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識別 | |
CAS號 | 19627-30-6 |
性質 | |
化學式 | C16H16O3S |
摩爾質量 | 288.36 g·mol−1 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
對甲苯磺酸肉桂酯是一種有機化合物,化學式為C16H16O3S。它可由對甲苯磺酸和肉桂醇在四氯化鋯[1]或磷鎢酸鋁[2]催化下反應製得。它和疊氮化鈉在二甲基甲醯胺中反應,可以得到肉桂基疊氮化物。[3]
參考文獻
- ^ Biswanath Das, Vtukuri Saidi Reddy. ZrCl 4 as an Efficient Catalyst for Selective Tosylation of Alcohols with p -Toluenesulfonic Acid. Chemistry Letters. 2004-11, 33 (11): 1428–1429 [2022-12-03]. ISSN 0366-7022. doi:10.1246/cl.2004.1428 (英語).
- ^ Razieh Fazaeli, Shahram Tangestaninejad, Hamid Aliyan. Solvent-free and selective tosylation of alcohols and phenols with p -toluenesulfonyl chloride by heteropolyacids as highly efficient catalysts. Canadian Journal of Chemistry. 2006-05-01, 84 (5): 812–818 [2022-12-03]. ISSN 0008-4042. doi:10.1139/v06-066. (原始內容存檔於2019-02-28) (英語).
- ^ Linwei Zeng, Jiaming Li, Sunliang Cui. Rhodium‐Catalyzed Atroposelective Click Cycloaddition of Azides and Alkynes. Angewandte Chemie International Edition. 2022-07-11, 61 (28) [2022-12-03]. ISSN 1433-7851. doi:10.1002/anie.202205037. (原始內容存檔於2022-12-03) (英語).
拓展閱讀
- Hirofumi Ochiai, Yoshinao Tamaru, Kazunori Tsubaki, Zenichi Yoshida. Unsaturated ester synthesis via copper(I)-catalyzed allylation of zinc esters. The Journal of Organic Chemistry. 1987-09, 52 (19): 4418–4420 [2022-12-03]. ISSN 0022-3263. doi:10.1021/jo00228a059. (原始內容存檔於2022-12-03) (英語).