雙環［2.2.2］辛烯
雙環[2.2.2]辛烯是一種有機化合物，化學式為C8H12。它可以1,3-環己二烯為原料，經N-雙環[2.2.2]辛亞基對甲苯磺酰肼中間體製得。[2]它和溴化氫在乙酸中反應，可以得到2-溴雙環[2.2.2]辛烷。[3]它可以被氫氣或肼還原為雙環[2.2.2]辛烷。[4][5]
| 雙環［2.2.2］辛烯 | |
|---|---|
octene.svg)
| |
| 識別 | |
| CAS號 | 931-64-6 
|
| 性質 | |
| 化學式 | C8H12 |
| 摩爾質量 | 108.18 g·mol−1 |
| 密度 | 0.9097 g·cm−3（0 °C）[1] |
| 沸點 | 136.5~139 °C[1] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
參考文獻
- ^ 1.0 1.1 Willstatter, Richard; Veraguth, Hans. Cyclooctane Series. II. Communication. Berichte der Deutschen Chemischen Gesellschaft, 1907. 40: 959-970.
- ^ John E. Baldwin, Phyllis A. Leber, David C. Powers. Thermal Reactions of 7- d - and 8- d -Bicyclo[4.2.0]oct-2-enes. Journal of the American Chemical Society. 2006-08-01, 128 (31): 10020–10021 [2021-11-12]. ISSN 0002-7863. doi:10.1021/ja0636035 （英語）.
- ^ Germain, J. E.; Blanchard, M. Isomerization of bicyclic olefins C8H12 on a silicophosphoric catalyst. Bulletin de la Societe Chimique de France, 1960: 473-481.
- ^ Brockway, Nolan M. Reactions of carbethoxycarbene with carbon-halogen bonds. Polar addition of deuterium bromide to bicyclo[2.2.2]-octene [Dissertation]. 1970. Univ. Oklahoma.
- ^ Hao Chen, Jianmin Wang, Xuechuan Hong, Hai-Bing Zhou, Chune Dong. A simple and straightforward approach toward selective C=C bond reduction by hydrazine. Canadian Journal of Chemistry. 2012-09, 90 (9): 758–761 [2021-11-12]. ISSN 0008-4042. doi:10.1139/v2012-057 （英語）.