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2-Diphenylphosphinobenzaldehyde

From Wikipedia, the free encyclopedia
2-Diphenylphosphinobenzaldehyde
Names
Preferred IUPAC name
2-(Diphenylphosphanyl)benzaldehyde
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.156.047 Edit this at Wikidata
UNII
  • InChI=1S/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
    Key: DRCPJRZHAJMWOU-UHFFFAOYSA-N
  • 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
    Key: DRCPJRZHAJMWOU-UHFFFAOYAH
  • C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3C=O
Properties
C19H15OP
Appearance yellow solid
Melting point 118 to 119 °C (244 to 246 °F; 391 to 392 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

2-Diphenylphosphinobenzaldehyde is a phosphine ligand with the formula (C6H5)2PC6H4CHO. It is a yellow solid that dissolves in common organic solvents.

Synthesis and reactions

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2-Diphenylphosphinobenzaldehyde was first prepared by the reaction of chlorodiphenylphosphine with the Grignard reagent derived from the protected 2-bromobenzaldehyde, followed by deprotection.[1][2] It can also be derived from (2-lithiophenyl)diphenylphosphine.

The compound condenses with a variety of amines to give phosphine-imine and phosphine-amine ligands.[3][4]

References

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  1. ^ Hoots, John E.; Rauchfuss, Thomas B.; Wrobleski, Debra A.; Knachel, Howard C. (2007). "39. Substituted Triaryl Phosphines". Inorganic Syntheses. pp. 175–179. doi:10.1002/9780470132524.ch39. ISBN 9780470132524.
  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.
  3. ^ Degrado, Sylvia J.; Mizutani, Hirotake; Hoveyda, Amir H. (2001). "Modular Peptide-Based Phosphine Ligands in Asymmetric Catalysis: Efficient and Enantioselective Cu-Catalyzed Conjugate Additions to Five-, Six-, and Seven-Membered Cyclic Enones". Journal of the American Chemical Society. 123 (4): 755–756. doi:10.1021/ja003698p. PMID 11456598.
  4. ^ Hu, Anjing; Zhang, Zhan-Ming; Xiao, Yuanjing; Zhang, Junliang (2020). "Stereoselective Synthesis of Chiral Sulfinamide Monophosphine Ligands (Ming-Phos)(S, Rs)-M". Organic Syntheses. 97: 262–273. doi:10.15227/orgsyn.097.0262. S2CID 235020219.