4-甲酰基苯甲酸
4-甲酰基苯甲酸 | |
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IUPAC名 4-Formylbenzoic acid | |
系统名 4-Formylbenzenecarboxylic acid | |
识别 | |
CAS号 | 619-66-9 |
PubChem | 12088 |
ChemSpider | 11591 |
SMILES |
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InChI |
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InChIKey | GOUHYARYYWKXHS-UHFFFAOYAP |
EINECS | 210-607-4 |
性质 | |
化学式 | C8H6O3 |
摩尔质量 | 150.13 g·mol−1 |
外观 | 白色固体 |
熔点 | 248 °C(521 K)(分解)[1] |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
4-甲酰基苯甲酸是一种有机化合物,化学式为OCHC6H4CO2H。它可作为对二甲苯氧化的副产物生成。[2]1,4-苯二甲醛和二氧化碳在碳酸钾的存在下于DMSO中反应,反应完成后酸化,也能得到4-甲酰基苯甲酸。[3]它和N,N'-二甲基乙二胺在三氟甲磺酸铜的催化下反应,可以得到4-(1,3-二甲基-2-咪唑烷基)苯甲酸。[4]
参考文献
- ^ Ross Stewart, L. G. Walker. THE POLAR EFFECT OF THE β-NITROVINYL GROUP. Canadian Journal of Chemistry. 1957-12-01, 35 (12): 1561–1569 [2021-06-29]. ISSN 0008-4042. doi:10.1139/v57-204 (英语).
- ^ H. Falcon, J.M. Campos-Martin, S.M. Al-Zahrani, J.L.G. Fierro. Liquid-phase oxidation of p-xylene using N-hydroxyimides. Catalysis Communications. 2010-10, 12 (1): 5–8 [2021-06-29]. doi:10.1016/j.catcom.2010.07.010. (原始内容存档于2018-06-25) (英语).
- ^ Liuqun Gu, Yugen Zhang. Unexpected CO 2 Splitting Reactions To Form CO with N -Heterocyclic Carbenes as Organocatalysts and Aromatic Aldehydes as Oxygen Acceptors. Journal of the American Chemical Society. 2010-01-27, 132 (3): 914–915 [2021-06-29]. ISSN 0002-7863. doi:10.1021/ja909038t (英语).
- ^ Juliana G. Pereira, João P. M. António, Ricardo Mendonça, Rafael F. A. Gomes, Carlos A. M. Afonso. Rediscovering aminal chemistry: copper( ii ) catalysed formation under mild conditions. Green Chemistry. 2020, 22 (21): 7484–7490 [2021-06-29]. ISSN 1463-9262. doi:10.1039/D0GC01977A (英语).