Hydrazone

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File:Hydrazone-2D.png
Structure of the hydrazone functional group

Hydrazones are a class of organic compounds with the structure Template:Chem2.<ref>Template:JerryMarch</ref> They are related to ketones and aldehydes by the replacement of the oxygen =O with the =Template:Chem2 functional group. They are formed usually by the action of hydrazine on ketones or aldehydes.<ref>Template:OrgSynth</ref><ref name="acetone">Template:OrgSynth</ref>

SynthesisEdit

Hydrazine, organohydrazines, and 1,1-diorganohydrazines react with aldehydes and ketones to give hydrazones.

Hydrazone synthesis

Phenylhydrazine reacts with reducing sugars to form hydrazones known as osazones, which was developed by German chemist Emil Fischer as a test to differentiate monosaccharides.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref>

UsesEdit

File:Pigment Yellow 97.svg
Pigment Yellow 97, a popular yellow colorant, is a hydrazone.<ref>Template:Cite journal</ref>

Hydrazones are the basis for various analyses of ketones and aldehydes. For example, dinitrophenylhydrazine coated onto a silica sorbent is the basis of an adsorption cartridge. The hydrazones are then eluted and analyzed by high-performance liquid chromatography (HPLC) using a UV detector.

The compound carbonyl cyanide-p-trifluoromethoxyphenylhydrazone (abbreviated as FCCP) is used to uncouple ATP synthesis and reduction of oxygen in oxidative phosphorylation in molecular biology.

Hydrazones are the basis of bioconjugation strategies.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> Hydrazone-based coupling methods are used in medical biotechnology to couple drugs to targeted antibodies (see ADC), e.g. antibodies against a certain type of cancer cell. The hydrazone-based bond is stable at neutral pH (in the blood), but is rapidly destroyed in the acidic environment of lysosomes of the cell. The drug is thereby released in the cell, where it exerts its function.<ref>Template:Cite journal</ref>

ReactionsEdit

Hydrazones are susceptible to hydrolysis:

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Alkyl hydrazones are 102- to 103-fold more sensitive to hydrolysis than analogous oximes.<ref>Template:Cite journal</ref>

When derived from hydrazine itself, hydrazones condense with a second equivalent of a carbonyl to give azines:<ref name="OrgSynth">Template:OrgSynth</ref>

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Hydrazones are intermediates in the Wolff–Kishner reduction.

Hydrazones are reactants in hydrazone iodination, the Shapiro reaction, and the Bamford–Stevens reaction to vinyl compounds. Hydrazones can also be synthesized by the Japp–Klingemann reaction via β-keto acids or β-keto-esters and aryl diazonium salts. Hydrazones are converted to azines when used in the preparation of 3,5-disubstituted 1H-pyrazoles,<ref>Template:Cite journal</ref> a reaction also well known using hydrazine hydrate.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> With a transition metal catalyst, hydrazones can serve as organometallic reagent surrogates to react with various electrophiles.<ref>Template:Cite journal</ref>

File:Lasri condensation reaction.svg

N,N-dialkylhydrazonesEdit

{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}} In N,N-dialkylhydrazones<ref>Template:Cite journal</ref> the C=N bond can be hydrolysed, oxidised and reduced, the N–N bond can be reduced to the free amine. The carbon atom of the C=N bond can react with organometallic nucleophiles. The alpha-hydrogen atom is more acidic by 10 orders of magnitude compared to the ketone and therefore more nucleophilic. Deprotonation with for instance lithium diisopropylamide (LDA) gives an azaenolate which can be alkylated by alkyl halides.<ref>Template:Cite journal</ref> The hydrazines SAMP and RAMP function as chiral auxiliary.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref>

SAMP RAMP chiral auxiliaries

Recovery of carbonyl compounds from N,N-dialkylhydrazonesEdit

Several methods are known to recover carbonyl compounds from N,N-dialkylhydrazones.<ref>Template:Cite journal</ref> Procedures include oxidative, hydrolytic or reductive cleavage conditions and can be compatible with a wide range of functional groups.

GalleryEdit

See alsoEdit

ReferencesEdit

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Template:Functional group Template:Hydrazines

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