| 词条 | Glutaconaldehyde |
| 释义 |
| verifiedrevid = 423027948 | ImageFile = Glutaconaldehyde.png | IUPACName = 5-Hydroxy-2,4-pentadienal | OtherNames = Glutacondialdehyde; Glutaconic aldehyde; Glutaconic dialdehyde; Pentenedial | Section1 = {{Chembox Identifiers | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 4779496 | InChI = 1/C5H6O2/c6-4-2-1-3-5-7/h1-6H/b3-1+,4-2+ | InChIKey = WFSXUTWNNVIIIG-ZPUQHVIOBI | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C5H6O2/c6-4-2-1-3-5-7/h1-6H/b3-1+,4-2+ | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = WFSXUTWNNVIIIG-ZPUQHVIOSA-N | CASNo = 821-42-1 | CASNo_Ref = {{cascite|correct|CAS}} | PubChem = 6011936 | SMILES = O=C\\C=C\\C=C\\O }} | Section2 = {{Chembox Properties | C=5|H=6|O=2 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} Glutaconaldehyde is an organic compound with the formula C5H6O2. It is an unsaturated dialdehyde as is related to glutaraldehyde and glutaconic acid, but exists in its enol form due to the conjugation with the double bond. Both the sodium and potassium salts of glutaconaldehyde are known. They are efficiently synthesized from pyridine sulfonate.[1][2] The reaction of the glutaconaldehyde anion with acid chlorides gives the corresponding enol esters.[1] Glutaconaldehyde can also be converted to the corresponding vinyl bromide as shown below.[3] This product can be reacted with nucleophiles, cross-coupled using palladium, or homologated by two carbons.[3][4] References1. ^1 {{cite journal | title = Über den Abbau des Pyridins zu Glutaconsäuredialdehyd und dessen Rückverwandlung in Pyridin (I.)| author = Baumgarten, P. | journal = Ber. Dtsch. Chem. Ges. | volume = 57 | issue = | pages = 1622 | year = 1924 | url = | doi =10.1002/cber.19240570876 }} 2. ^{{cite journal | title = Glutaconaldehyde Sodium Salt from Hydrolysis of Pyridinium-1-Sulfonate | author = Becher, J. | journal = Organic Syntheses | volume = 59 | issue = | pages = 79–84 | year = 1979 | url = | doi = }} 3. ^1 {{cite journal | title = 5-Bromopentadienal: A Versatile Intermediate for the Synthesis of Functionalized Polyenic Compounds |author1=Soullez, D. |author2=Ple, G. |author3=Duhamel, L. Duhamel P. | journal = J. Chem. Soc., Chem. Commun. | volume = | issue = | pages = 563–564 | year = 1995 | url = | doi = }} 4. ^{{cite journal | title = Application of (2E,4E)-5-Bromo-2,4-Pentadienal in Palladium Catalysed Cross-Coupling: Easy Access to (2E,4E)-2,4-Dienals |author1=Vicart, N. |author2=Castet-Caillabet, D. |author3=Ramondenc, Y. |author4=Ple, G. |author5=Duhamel, L. | journal = Synlett | volume = | issue = | pages = 411–412 | year = 1998 | url = | doi = }} 1 : Aldehydes |
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