Transcript Important (and sometimes forgotten organic transformations)

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Important
(and sometimes forgotten)
organic transformations
Original idea from Macmillan group presentation:
http://www.princeton.edu/chemistry/macmillan/groupmeetings/BDH_important%20forgotten.pdf
Other good sites: http://www.chem.ox.ac.uk/thirdyearcomputing/NOR-oxford.asp
Nadia Fleary-Roberts
8/02/12
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Sandmeyer reaction
•Synthesis of aryl halides via diazoninum salts
Advantages
Limitations
•Can access substitution patterns
otherwise unachievable by direct
substitution
•Addition of hypophosphorous acid
(H3PO2) can result in dediazonization
(H-substitution)
Mechanism
Sandmeyer, T. Ber. 1884, 17, 1633-1635.
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Echenmoser fragmentation
•Formation of a ketone and an alkyne from the fragmentation of an epoxide using
TsNHNH2
•Reaction starts with formation of tosylhydrazone
A Eschenmoser et al, Helv. Chim. Acta 50, 708 (1967)
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Fischer Indole synthesis
•Requires acid catalysis and elevated temperatures
Larock indole synthesis
•The presence of alcohol groups in the alkyne seems to have a particularly strong
directing effect
•catalytic process involves arylpalladium formation, regioselective addition to the C-C
triple bond of the alkyne, and subsequent intramolecular palladium displacement.
Larock, R.; Yum, E.K. J. Am. Chem. Soc. 1991, 113, 6689
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Vilsmeier-Haack reaction
formylation of electron-rich arenes.
•The formylating (Vilsmeir) reagent is formed in-situ from DMF
•Followed by electrophilic aromatic substitution and hydrolysis
Haack, A. Ber, 1927, 60, 119
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Pummerer reaction
•Rearrangement of an alkyl sulfoxide to an α-substituted sulfide
•Common nucleophiles are carboxylates, amides, alkenes and phenols
•Pummerer fragmentation occurs when the α- group eliminates instead
R. Pummerer, Chem. Ber., 1909, 42, 2282; R. Pummerer, Chem. Ber.,
1910, 43, 1401; Jérôme Lacour Chem Commun, 2006, 2786–2788,
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Barton McCombie reaction
•Deoxygenation of alcohols
•Xanthate ester is formed first
•Driving force is the formation of very stable S-Sn bonds
•Tertiary alcohols are prone to elimination (Chugaev reaction)
•Thionoformates may be used to derivatise and deoxygenate tertiary alcohols
without competing elimination
Barton, D. H. R; McCombie, S. W. 1975. J. Chem. Soc., Perkin Trans. 1, 16: 1574–1585
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Prevost reaction
•Synthesis of anti-diols from alkenes
•neighbouring-group participation mechanism prevents the immediate nucleophilic substitution
of iodine by a second equivalent of benzoate that would lead to a syn-substituted product.
The Ag+ helps to make iodine a better leaving group
•The Woodward modification can be used to make syn-diols
Woodward modification
•Reagents used are iodine and silver acetate in wet acetic acid
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Baylis-Hillman reaction
•Phosphines can also be used
•DMAP and DBU are better in some cases
•Other mechanism proposed: JOC, 2005, 70, 3980
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dr: 64:36
Zhu, EJOC: 2003, 1133-1144
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Ugi reaction
•Multi-component reaction between a ketone or aldehyde, an amine, an isocyanide
and a carboxylic acid
•Useful for forming compound libraries
Mechanistic steps
1. Imine formation
2. Protonation of imine by
acid
3. α-addition of
carboxylate and
imimium ion to the
isocyanide
4. Intramolecular acyl
transfer
Ugi, I. ACIE. 1962. 1,8.
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Zweifel Olefin synthesis
•Synthesis of trans alkenes via hydroboration-cyanohalogenation
•Hydroboration of an alkyne to form a vinyl borane which can then undergo reductive
elimination
•Hydroboration, alkyl migration and B-X elimination are all stereospecific
Zweifel, G.; Fisher, R. P.; Snow, J. T.; Whitney, C. C. J. Am. Chem. Soc. 1972, 94, 6560-6571
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Polonovski reaction
•Rearrangement of a tertiary N-oxide activated by Ac2O to form an N,Ndisubstituted acetamide and an aldehyde
•Other activating agents such as chloroformate esters, acid chlorides, iron
salts and sulfur dioxide can be used.
M. Polonovski, Bull. Soc. Chim. France 41, 1190 (1927).
•The Polonovski-Potier modification uses TFAA
Cave et al., Tetrahedron 23, 4681 (1967);
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Wolff rearrangement/ArndtEistert reaction
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Cannizzaro reaction
•Only works with unenolizable aldehydes
Clayden pg: 713
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Kornblum oxidation
•Oxidative cleavage of carbon-halogen bond
•Reaction of a primary halide/triflate with DMSO to form an aldehyde
•Modification involves treatment of the primary halide with silver tosylate
followed by DMSO and the base.
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Ponndorf (Meerwein-Verley) reduction
•Reduction of ketones/aldehydes to alcohols
•The reverse reaction is known as the Oppenauer oxidation
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Seyferth-Gilbert Homologation
•Base promoted homologation of aldehydes to alkynes
•The Ohira-Bestmann modification allows the use of milder bases
(K2CO3)
Gilbert J. Org. Chem., 1982, 47, 1837-1845
Ohira, Synth. Commun., 1986, 19, 561.
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Wolff-Kishner reduction
•Reduction of aldehydes/ketones to alkanes
•The hydrazone is formed first and then treated with base
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Me3SiCl, LDA
Pd(OAc)2, MeCN
25 °C, 60 h
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Saegusa Oxidation
•conversion of a silyl enol ether functional group into the corresponding
α, β unsaturated enone
•The oxidising agent palladium (II) acetate is used in stoichiometric
amounts
Y. Ito et al., J. Org. Chem. 43, 1011 (1978)