正丁基钠
正丁基钠是一种有机钠化合物,化学式为C4H9Na,它具有强碱性,为聚合结构。它可由正丁基锂和叔丁醇钠反应制得。[2]它和1-溴萘反应,可以得到1-溴丁烷和1-萘基钠。[3]
正丁基钠 | |
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IUPAC名 | |
别名 | 丁基钠 |
识别 | |
CAS号 | 3525-44-8 |
PubChem | 101040259 |
ChemSpider | 11351318 |
SMILES |
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InChI |
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InChIKey | IRDQNLLVRXMERV-UHFFFAOYSA-N |
性质 | |
化学式 | C4H9Na |
摩尔质量 | 80.1 g·mol−1 |
外观 | 白色固体[1] |
危险性 | |
GHS危险性符号 | |
GHS提示词 | 危险 |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
参考文献
编辑- ^ Martinez-Martinez, A. J.; Kennedy, A. R.; Mulvey, R. E.; O'Hara, C. T. Supplementary Material for Directed ortho-meta'- and meta-meta'-dimetalations: A template base approach to deprotonation. Science. 13 November 2014, 346 (6211): 834–837 [2024-09-10]. Bibcode:2014Sci...346..834M. PMID 25395533. S2CID 206561570. doi:10.1126/science.1259662. (原始内容存档于2022-04-30).
- ^ Schade, Christian; Bauer, Walter; Von Ragué Schleyer, Paul (November 1985). "n-Butylsodium: The preparation, properties and NMR spectra of a hydrocarbon- and tetrahydrofuran-soluble reagent". Journal of Organometallic Chemistry. 295 (3): c25–c28. doi:10.1016/0022-328X(85)80326-0
- ^ Gilman, Henry; Moore, Fred W.; Baine, Ogden (September 1941). "Secondary and Tertiary Alkyllithium Compounds and Some Interconversion Reactions with Them". Journal of the American Chemical Society. 63 (9): 2479–2482. doi:10.1021/ja01854a046