Chemistry:2-Carboxybenzaldehyde

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2-Carboxybenzaldehyde
2-Carboxybenzaldehyd Struktur.svg
Names
Preferred IUPAC name
2-Formylbenzoic acid
Other names
2-Phthaldehydic acid
Identifiers
3D model (JSmol)
742381
ChEBI
ChEMBL
ChemSpider
EC Number
  • 204-342-3
UNII
Properties
C8H6O3
soluble[1]
Solubility soluble in diethylether, ethanol[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Tracking categories (test):

2-Carboxybenzaldehyde is a chemical compound. It consists of a benzene ring, with an aldehyde and a carboxylic acid as substituents that are ortho to each other. The compound exhibits ring–chain tautomerism: the two substituents can react with each other to form 3-hydroxyphthalide, a cyclic lactol. This lactol reacts readily with Grignard reagents , forming alkyl- and aryl-substituted phthalides.[2] Other benzo-fused heterocyclic compounds can be derived from 2-carboxybenzaldehyde, including isoindolinones and phthalazinones, with a variety of pharmacological properties, such as the antihistamine azelastine.

Synthesis

2-Carboxybenzaldehyde was first prepared from phthalide and characterized in 1887.[3] The reaction of bromine with phthalide produces 2-bromophthalide, which is converted into 2-formylbenzoic acid by heating with water in a total yield of 78 to 83%.[4]

Synthese von 2-Carboxybenzaldehyd aus Phthalid

An analogous process based on a chlorination reaction can also be used:[5]

2-Carboxybenzaldehyd from Phthalide via chlorination.png

The synthesis of 1-dichloromethyl-2-(trichloromethyl)benzene by photochlorination of o-xylene was also reported in 1887.[6]

Synthese von 2-Carboxybenzaldehyd aus o-Xylol

The hydrolysis of the pentachloroxylene to the 2-carboxybenzaldehyde is carried out by boiling it with FeCl3-containing hydrochloric acid.[7]

In the reaction of phthalic anhydride with sodium tetracarbonylferrate, only one of the carboxyl groups is reduced to the aldehyde, the second remains unchanged.[8]

Synthese von 2-Carboxybenzaldehyd aus Phthalsäureanhydrid

This gives 2-carboxybenzaldehyde in a yield of 61%.

In a laboratory procedure, the oxidation of naphthalene with alkaline potassium permanganate is given, which, however, yields only a yield of 39% 2-carboxybenzaldehyde.[9] Also the oxidation of naphthalene with ozone to 2-formylbenzoic acid offers no significant advantages.[10]

Synthese von 2-Carboxybenzaldehyd aus Naphthalin

Properties

Pure 2-carboxybenzaldehyde is a white crystalline powder which dissolves in water and in short-chain alcohols. In solid form and in most solvents, the substance is present as racemic 3-hydroxyphthalide (a lactol) as a result of ring–chain tautomerism.[7]

Gleichgewicht 2-Carboxybenzaldehyd-3-Hydroxyphthalid

The refractive index is = 1.4500 (at 25 °C, 589 nm).[11]

Application

In the lactol form, 2-carboxybenzaldehyde behaves like a carboxylic acid anhydride and reacts smoothly with alcohols forming 3-alkoxyphthalides.[7]

Reaktion von 3-Hydroxyphthalid mit Nukleophilen

Also with other nucleophilic compounds, such as, thiols, amines, amides, etc., 3-hydroxyphthalide reacts without a catalyst to give the corresponding derivatives.[7] For example, it reacts with morpholine in 91% yield to 3-morpholinyl phthalide.[12] 3-Hydroxyphthalide reacts with thionyl chloride at the hydroxyl group smoothly (80-90% yield) to 3-chlorophthalide.[12] With Grignard reagents, the hydroxy group can be exchanged for the corresponding alkyl or aryl group:[2]

Reaktion von 3-Hydroxyphthalid mit Grignard-Verbindungen

In the presence of (+)-cinchonine, in the reaction of (racemic) 3-hydroxyphthalide with carboxylic acid anhydrides to the corresponding chiral 3-substituted phthalides an enantiomeric excess of up to 90% ee can be achieved besides high product yields.[13] An alternative approach to (racemic) 3-substituted phthalides with high yields is opened up by the reaction of 2-carboxybenzaldehyde and β-keto acids in the presence of base 4-anisidine in glycerol as solvent.[14]

Reaktion von 3-Hydroxyphthalid mit β-Ketosäuren

2-Carboxybenzaldehyde underdoes a double condensation reaction with hydrazine or alkylhydrazines, 1(2H)-phthalenazinones are obtained under acid catalysis with K10-montmorillonite and microwave irradiation in high yield.[15]

Reaktion von 2-Carboxybenzaldehyd mit Alkylhydrazinen

Phthalazinones (1(2H)-phthalenazinones) are important building blocks for natural products, fine chemicals and pharmaceutical active ingredients,[16] such as the antihypertensive vasodilator hydralazine.[5]

2-carboxybenzaldehyde can also be used for the preparation of N-substituted isoindolinones (1-isoindolinones, 2,3-dihydroindol-1-ones) which are formed when reacting 2-carboxybenzaldehyde with primary amines in the presence of platinum nanowires and low hydrogen pressure in 1,4-dioxane in very high yields:[16]

Synthese von Isoindolinonen durch 3-Komponentenreaktion

When the reaction of 2-carboxybenzaldehyde is carried out with primary amines in the presence of dimethylphosphite, the corresponding isoindolin-1-one-3-phosphonates are obtained first. After activation with butyllithium with aromatic aldehydes (such as, benzaldehyde in a Horner-Wadsworth-Emmons reaction), these can be converted in very high yields to 3-(arylmethylene)isoindolin-1-ones.[17]

Synthese von Arylmethylenisoindolinonen

More recently, 2-formylbenzoic acid became due to its reactivity of some interest as versatile molecular building block in multicomponent reactions, for example the Ugi reaction, for the synthesis of heterocyclic annellated aromatics. Functionalized isoindolinones are accessible in high yields in a three-component reaction with 2-formylbenzoic acid and 2-bromoanilines by palladium-catalyzed carbonylation.[18]

Synthese von funktionalisierten Isoindolinonen

Another three-component reaction (here carried out as a Strecker synthesis) with 2-carboxybenzaldehyde, primary amines and potassium cyanide in methanol yields in the acidic medium an N-substituted isoindolinone-1-carbonitrile, formally an aminoacetonitrile derivative of isoindolinone with two moles of HCN.[19]

Synthese von Isoindolinonen aus 2-Carboxybenzaldehyd via Strecker-Synthese

When substituted 2-formylbenzoic acid, potassium cyanide and equimolar amounts of primary aromatic amines and acetic acid are used, substituted isochromes-1-ones (isocumarins, 1H-2-benzopyran-1-ones) are obtained in good yields.[20]

Synthese von Isochromenonen durch 3-Komponentenreaktion mit Kaliumcyanid

The isochromenones obtained are quantitatively converted into isoindolinones by reacting in DMSO upon ring constriction into substituted isobenzofurans or with catalytic amounts of iodine in triethylamine.[21]

With isonitriles instead of potassium cyanide, 2-carboxybenzaldehyde and primary aromatic amines react in methanol to form substituted isochromen-1-ones, which are converted to isoindolinones with traces of acid.[22]

Synthese von Isochromenonen durch 3-Komponentenreaktion mit Isocyaniden

Synthesis pathways for the isoquinoline derivative[23] quinisocaine[24] (acting as a local anesthetic) and the antihistamine azelastine[25] are also based on 2-carboxybenzaldehyde as starting material.

References

  1. ↑ 1.0 1.1 William M. Haynes (2016), CRC Handbook of Chemistry and Physics, 97th Edition, Boca Raton, FL, U.S.A.: CRC Press, pp. 3–278, ISBN 978-1-4987-5429-3 
  2. ↑ 2.0 2.1 P. Cannone; J. Plamondon; M. Akssira (1988), "Reactions selectives de organomagnesiens avec les lactols et les lactones. Synthese des diols primaires-secondaires", Tetrahedron 44 (10): 2903–2912, doi:10.1016/S0040-4020(88)90027-0 
  3. ↑ S. Racine (1887), "VIII. Ueber Phthalaldehydsäure" (in German), Justus Liebigs Ann. Chem. 239 (1): 78–91, doi:10.1002/jlac.18872390106, https://zenodo.org/record/1427413 
  4. ↑ "Phthalaldehydic acid". Organic Syntheses. doi:10.15227/orgsyn.023.0074. 
  5. ↑ 5.0 5.1 J. Druey; B.H. Ringier (1951), "21. Hydrazinderivate der Phthalazin- und Pyridazinreihe" (in German), Helv. Chim. Acta 34 (1): 195–210, doi:10.1002/hlca.19510340122 
  6. ↑ A. Colson; H. Gautier (1887), "Nouveau mode de chloruration des carbures", Ann. Chim. Phys. 6 (11): 19–32 
  7. ↑ 7.0 7.1 7.2 7.3 D.D. Wheeler; D.C. Young; D.S. Erley (1957), "Reactions of phthalaldehydic acid", J. Org. Chem. 22 (5): 547–556, doi:10.1021/jo01356a022 
  8. ↑ Y. Watanabe; M. Yamashita; T-a. Mitsudo; M. Tanaka; Y. Takegami (1973), "The facile synthesis of aldehydes and aldehydic acids from carboxylic acid anhydrides using sodium tetracarbonylferrate", Tetrahedron Lett. 14 (37): 3535–3536, doi:10.1016/S0040-4039(01)86963-X 
  9. ↑ "Phthalaldehydic acid". Organic Syntheses. doi:10.15227/orgsyn.016.0068. 
  10. ↑ L. Seekles (1924), "Ortho phthalaldehydic acid", Rec. Trav. Chim. 43 (5): 329–340, doi:10.1002/recl.19240430506 
  11. ↑ Carl L. Yaws (2015), Thermophysical Properties of Chemicals and Hydrocarbons, 2nd Edition, Oxford, UK: Elsevier Inc., p. 183, ISBN 978-0-323-28659-6 
  12. ↑ 12.0 12.1 K.B. Sloan; S.A.M. Koch (1983), "Effect of Nucleophilicity and Leaving Group Ability on the SN2 Reactions of Amines with (Acyloxy)alkyl α-Halides: A Product Distribution Study", J. Org. Chem. 48 (5): 635–640, doi:10.1021/jo00153a002 
  13. ↑ D. Niedek; S.M.M. Schuler; C. Eschmann; R.C. Wende; A. Seitz; F. Keul; P.R. Schreiner (2017), "Synthesis of enantioenriched phthalides and isoindolinone derivatives from 2-formylbenzoic acid", Synthesis 49 (2): 371–382, doi:10.1055/s-0036-1589404 
  14. ↑ L. Jia; F. Han (2017), "Sustainable synthesis of 3-substituted phthalides via a catalytic one-pot cascade strategy from 2-formylbenzoic acid with β-keto acids in glycerol", Beilstein J. Org. Chem. 13: 1425–1429, doi:10.3762/bjoc.13.139, PMID 28781708 
  15. ↑ V.M. Outerbridge; S.M. Landge; H. Tamaki; B. Török (2009), "Microwave-promoted solid-acid-catalyzed one-pot synthesis of phthalazinones", Synthesis 2009 (11): 1801–1806, doi:10.1055/s-0028-1088074 
  16. ↑ 16.0 16.1 L. Shi; L. Hu; J. Wang; X. Cao; H. Gu (2012), "Highly efficient synthesis of N-substituted isoindolinones and phthalazinones using Pt nanowires as catalysts", Org. Lett. 14 (7): 1876–1879, doi:10.1021/ol300471a, PMID 22420427 
  17. ↑ M.A. Reyes-Gonzàlez; A. Zamundio-Medina; M. Ordónez (2012), "Practical and highly selective synthesis of 3-(arylmethylene)isoindolin-1-ones from 2-formylbenzoic acid", Tetrahedron Lett. 53 (43): 5756–5758, doi:10.1016/j.tetlet.2012.08.040 
  18. ↑ K. Natte; J. Chen; H. Li; H. Neumann; M. Beller; X.F. Wu (2014), "Palladium-catalyzed carbonylation of 2-bromoanilines with 2-formylbenzoic acid and 2-halobenzaldehydes: Efficient synthesis of functionalized isoindolinones", Chem. Eur. J. 20 (44): 14184–14188, doi:10.1002/chem.201404446, PMID 25212125 
  19. ↑ T. Opatz; D. Ferenc (2004), "An unexpected three-component condensation leading to amino-(3-oxo-2,3-dihydro-1H-isoindol-1-ylidene)-acetonitriles", J. Org. Chem. 69 (24): 8496–8499, doi:10.1021/jo0486802, PMID 15549828 
  20. ↑ T. Opatz; D. Ferenc (2005), "Facile preparation of 3-amino-4-(arylamino)-1H-isochromen-1-ones by a new multi-component reaction", Eur. J. Org. Chem. 2005 (5): 817–821, doi:10.1002/ejoc.200400685 
  21. ↑ T. Opatz; D. Ferenc (2006), "Ring contracting rearrangements of 3-amino-4-(arylamino)-1H-isochromen-1-ones", Eur. J. Org. Chem. 1: 121–126, doi:10.1002/ejoc.200500575 
  22. ↑ C. Faggi; M. Garcia-Valverde; S. Macaccini; G. Menchi (2010), "Isolation of Ugi four-component condensation primary adducts: A straightforward route to isocoumarins", Org. Lett. 12 (4): 788–791, doi:10.1021/ol9028622, PMID 20104888 
  23. ↑ J.W. Wilson; N.D. Dawson; W. Brooks; G.E. Ullyot (1949), "Local anesthetics. Aminoalkoxyisoquinoline derivatives", J. Am. Chem. Soc. 71 (3): 937–938, doi:10.1021/ja01171a047, PMID 18129083 
  24. ↑ (in German) Hagers Handbuch der Pharmazeutischen Praxis, 5. Aufl., Berlin: Springer, 1994, p. 482, doi:10.1007/978-3-642-57880-9, ISBN 978-3-642-63389-8 
  25. ↑ G. Scheffler; J. Engel; B. Kutscher; W.S. Sheldrick; P. Bell (1988), "Synthese und Kristallstrukturanalyse von Azelastin" (in German), Arch. Pharm. 321 (4): 205–208, doi:10.1002/ardp.19883210406 



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