2-二苯基膦基苯甲醛

化合物

2-二苯基膦基苯甲醛是一種有機磷化合物,化學式為(C6H5)2PC6H4CHO。它是黃色固體,可溶於常見的有機溶劑中。它和可以發生縮合反應,得到一系列膦-亞胺或膦-胺類配體[1]它最初由二苯基氯化膦和含保護基的溴苯甲醛的格氏試劑反應,脫保護後得到。[2](2-鋰基苯基)二苯基膦也能轉化至該化合物。

2-二苯基膦基苯甲醛
IUPAC名
2-diphenylphosphanylbenzaldehyde
識別
CAS號 50777-76-9  checkY
PubChem 2754316
ChemSpider 2035266
SMILES
 
  • C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3C=O
InChI
 
  • 1/C19H15OP/c20-15-16-9-7-8-14-19(16)21(17-10-3-1-4-11-17)18-12-5-2-6-13-18/h1-15H
InChIKey DRCPJRZHAJMWOU-UHFFFAOYAH
性質
化學式 C19H15OP
外觀 黃色固體
熔點 118—119 °C(391—392 K)
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

它和金屬形成的配合物是已知的。[3]

參考文獻

編輯
  1. ^ S. J. Degrado, H. Mizutani and A. H. Hoveyda, "Modular Peptide-Based Phosphine Ligands in Asymmetric Catalysis: Efficient and Enantioselective Cu-Catalyzed Conjugate Additions to Five-, Six-, and Seven-Membered Cyclic Enones", J. Am. Chem. Soc. 2001, volume 123, pp. 755-756. doi:10.1021/ja003698p
  2. ^ Schiemenz, Guenter P.; Kaack, Hermann "Aromatische Phosphine mit Substituenten zweiter Ordnung, XIII. Triarylphosphine mit mehreren Carbonyl-Funktionen durch Grignard-Synthese (Aromatic phosphines with second order substituents. XIII. Preparation of triarylphosphines with several carbonyl functions by Grignard synthesis)" Justus Liebigs Annalen der Chemie 1973, vol. 9, pp. 1480-93. doi:10.1002/jlac.197319730910. Hoots, J. E., Rauchfuss, T. B., Wrobleski, D. A. "Substituted Triaryl Phosphines" Inorganic Syntheses, 1982, Volume 21, pp. 175. doi:10.1002/9780470132524.ch39
  3. ^ Adrian B. Chaplin, Joel F. Hooper, Andrew S. Weller, Michael C. Willis. Intermolecular Hydroacylation: High Activity Rhodium Catalysts Containing Small-Bite-Angle Diphosphine Ligands. Journal of the American Chemical Society. 2012-03-14, 134 (10): 4885–4897 [2020-12-22]. ISSN 0002-7863. doi:10.1021/ja211649a. (原始內容存檔於2019-01-12) (英語).