2-乙基噻吩
| 2-乙基噻吩 | |
|---|---|
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| 识别 | |
| CAS号 | 872-55-9 
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| SMILES |
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| 性质 | |
| 化学式 | C6H8S |
| 摩尔质量 | 112.19 g·mol−1 |
| 沸点 | 134-135 °C[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
2-乙基噻吩是一种有机硫化合物，化学式为C6H8S。它可由2-乙酰基噻吩加氢还原制得，[2]或由噻吩、正丁基锂、溴乙烷反应得到。[3]它和碘苯、碳酸银在催化下反应，可以得到2-乙基-5-苯基噻吩。[4]
参考文献[编辑]
- ^ Buu-Hoi, Ng. Ph.; Hoan, Nguyen; Khoi, Ng.-H. Potential nitrogen-heterocycle carcinogens. VII. Polycyclic carbazoles bearing ethyl groups, and thiophene isosters thereof. Journal of Organic Chemistry, 1950. 15: 957-961. ISSN 0022-3263.
- ^ Catalytic Reduction of 2-Acylthiophenes. J Am Chem Soc. 1951. 73 (11) doi:10.1021/ja01155a071
- ^ Oligothiophenes substituted with the thionitrile group: synthesis, characterization, and thin-film formation on gold substrates. Journal of Materials Chemistry. 2009. doi:10.1039/b908869e
- ^ Yanagisawa, Shuichi; Sudo, Tomoko; Noyori, Ryoji; Itami, Kenichiro. Direct C-H arylation of (hetero)arenes with aryl iodides via rhodium catalysis. J Am Chem Soc. 2006. doi:10.1021/ja064500p