Ketene rearrangement

Table 2. Insertion reaction, phosphene and ketene rearrangements of phosphorylacylcarbenes (37)...

The photolysis of cyclic diazo ketones in hydroxylic solvents leads to ring contracted carboxylic acid derivatives via this ketocarbene -> ketene rearrangement. Examples of such reactions are given in (2.24)239) and (2.25) 240). In this last example a photoequilibrium between the diazo ketone and its valence isomer, a diazirine, has been observed, both products then eliminating nitrogen to afford the cyclobutane carboxylic acid. 

The photochemistry of a,p nsaturated ketones has attracted much attention and is still a field cld of current interest. 1/Numer-ous examples of such photochemical transformations are well-documented for cyclic enones and dienones, including both cycloaddition ructions and rearrangements. For example, cyclopentenones / and/readily rearrange to cyclopropyl ketenes upon irra/idiation. Recently, the related cyclohexadienone/butadienyl ketene rearrangement has been shown to be a highly useful tool in the synthesis of natural products and macrocydic lactone /... 

In contrast to the carbene and carbenoid chemistry of simple diazoacetic esters, that of a-silyl-a-diazoacetic esters has not yet been developed systematically [1]. Irradiation of ethyl diazo(trimethylsilyl)acetate in an alcohol affords products derived from 0-H insertion of the carbene intermediate, Wolff rearrangement, and carbene- silene rearrangement [2]. In contrast, photolysis of ethyl diazo(pentamethyldisilanyl)acetate in an inert solvent yields exclusively a ketene derived from a carbene->silene->ketene rearrangement [3], Photochemically generated ethoxycarbonyltrimethyl-silylcarbene cyclopropanates alkenes and undergoes insertion into aliphatic C-H bonds [4]. Copper-catalyzed and photochemically induced cyclopropenation of an alkyne with methyl diazo(trimethylsilyl)acetate has also been reported [5]. 

Strausz, O. P., Gosavi, R. K., Gunning, H. E. Ab initio molecular orbital calculations on the reaction path of the ketocarbene-ketene rearrangement. J. Chem. Phys. 1977, 67, 3057-3060. 

The photoinduced Wolff rearrangement of 5-diazo-2,2-dimethyl-l,3-dioxan-4,6-dione has also been examined by TRIR methods [116], These ultrafast measurements, conducted in a PMMA matrix, revealed that the formation of the ketene rearrangement product was complete within 20 ps a carbonyl carbene was not detected in this study. Other applications of TRIR spectroscopy to the study of carbene-related chemistry include investigations of diazirine to diazo rearrangements [117] and of oxygen and sulfur atom transfer reactions [118]. 

Both types of reactivity of ynolate anion have been reported in the literature. The O-attack is typical for the reactions of lithium ynolates with trialkylchlorosilanes b24,25 dialkyIchlorophosphates. Lithium ynolates, generated as shown in equations 5-10, react with sterically hindered trialkylchlorosilanes in THF affording silyl ynol ethers as primary products (equation 12). However, in some cases the silyl ynol ethers are unstable at room temperature and isomerization to the more stable ketenes, or decomposition, occurs The ketene rearrangement usually occurs in reactions of lithium alkynolates with methyl substituted silyl chlorides a typical example of such a rearrangement is represented by reaction 13 ". ... 

According to Hooke s law calculation, the frequency of 2075 cm for the labeled ketene can be expected. Further thermolysis at 700 °C resulted in reduction by c. 50% in the intensity of the minor but characteristic peak at 2070 cm thus indicating that the ketene—ketene rearrangement 312a —> 312b occurs. Two products are obtained via the preparative FVT of 311 at 650 °C. They are identified as 4-benzoyloxyquinohne 316 (60%) and 4-quinolone 313 (30%). The initial electrocyclization of ketene... 

With higher aliphatic acids, RCOOH, keten yields first a mixed anhydride CH3COOCOR, which can be distilled under reduced pressure by slow distillation at atmospheric pressure the mixed anhydride undergoes rearrangement into the anhydride of the higher fatty acid and acetic acid, for example ... 

During this early period, a very ingenious free-radical route to polyesters was used to introduce weak linkages into the backbones of hydrocarbon polymers and render them susceptible to bio degradabihty (128—131). Copolymerization of ketene acetals with vinyl monomers incorporates an ester linkage into the polymer backbone by rearrangement of the ketene acetal radical as illustrated in equation 13. The ester is a potential site for biological attack. The chemistry has been demonstrated with ethylene (128—131), acryhc acid (132), and styrene (133). 

Acylation. Reaction conditions employed to acylate an aminophenol (using acetic anhydride in alkaU or pyridine, acetyl chloride and pyridine in toluene, or ketene in ethanol) usually lead to involvement of the amino function. If an excess of reagent is used, however, especially with 2-aminophenol, 0,A/-diacylated products are formed. Aminophenol carboxylates (0-acylated aminophenols) normally are prepared by the reduction of the corresponding nitrophenyl carboxylates, which is of particular importance with the 4-aminophenol derivatives. A migration of the acyl group from the O to the N position is known to occur for some 2- and 4-aminophenol acylated products. Whereas ethyl 4-aminophenyl carbonate is relatively stable in dilute acid, the 2-derivative has been shown to rearrange slowly to give ethyl 2-hydroxyphenyl carbamate [35580-89-3] (26). 

Production is by the acetylation of 4-aminophenol. This can be achieved with acetic acid and acetic anhydride at 80°C (191), with acetic acid anhydride in pyridine at 100°C (192), with acetyl chloride and pyridine in toluene at 60°C (193), or by the action of ketene in alcohoHc suspension. 4-Hydroxyacetanihde also may be synthesized directiy from 4-nitrophenol The available reduction—acetylation systems include tin with acetic acid, hydrogenation over Pd—C in acetic anhydride, and hydrogenation over platinum in acetic acid (194,195). Other routes include rearrangement of 4-hydroxyacetophenone hydrazone with sodium nitrite in sulfuric acid and the electrolytic hydroxylation of acetanilide [103-84-4] (196). 

Rearrangement (ring contraction) of a-diazokelones to cartioxylic adds or their derivatives (esters, amides) via ketenes (see also Amdt-Eistert). 

The photochemistry of cyclobutanones differs from that of less strained larger cycloalkanones. Fragmentation to ethylene and ketene (derivatives), decarbonylation and rearrangement to oxacarbenes predominate here. The oxacarbene formation, which occurs with retention of the configuration of the... 

The photolytic decomposition of a-diazoketones, accompanied by rearrangement to ketene (photolytic Wolff rearrangement), has been used successfully in the preparation of A-nor- and C-norsteroids. The method is reviewed in chapter 15 by R. M. Scribner. ... 

The methyl ester (100, R = CH3), derived from this A-nor acid by treatment with diazomethane, is different from the ester (102) obtained either by Favorskii rearrangement of 2a-bromo-5a-cholestan-3-one (101) or by the action of cyanogen azide on 3-methoxy-5a-cholest-2-ene (103) followed by hydrolysis on alumina. The ketene intermediate involved in photolysis of (99) is expected to be hydrated from the less hindered a-side of the molecule to give the 2j -carboxylic acid. The reactions which afford (102) would be expected to afford the 2a-epimer. These configurational assignments are confirmed by deuteriochloroform-benzene solvent shifts in the NMR spectra of esters (100) and (102). ... 

Sulfur tnoxide adds to 2,2 difluoroethylenesulfonyl fluoride to afford the P sultone and its rearrangement product, bis(fluorosulfonyl)acetyl fluoride Potassium fluoride acts as a base and reacts with the acetyl fluoride to eliminate the elements of hydrogen fluoride and produce bis(fluorosulfonyl)ketene [IS] (equation 6)... 

The diazo ketone 3, when treated with silver oxide as catalyst, decomposes into ketocarbene 5 and dinitrogen Na. This decomposition reaction can also be achieved by heating or by irradiation with uv-light. The ketocarbene undergoes a Wolff rearrangement to give a ketene 6 ... 

The ketocarbene 4 that is generated by loss of Na from the a-diazo ketone, and that has an electron-sextet, rearranges to the more stable ketene 2 by a nucleophilic 1,2-shift of substituent R. The ketene thus formed corresponds to the isocyanate product of the related Curtius reaction. The ketene can further react with nucleophilic agents, that add to the C=0-double bond. For example by reaction with water a carboxylic acid 3 is formed, while from reaction with an alcohol R -OH an ester 5 is obtained directly. The reaction with ammonia or an amine R -NHa leads to formation of a carboxylic amide 6 or 7 ... 

To illustrate the value of the mass spectra of the labeled compounds, the peaks at m/e 129 in Figures 7 and 8 will be considered first. These peaks could be from the loss of acetic acid (60 mass units) from m/e 189, or the loss of water (18 mass units) from m/e 189 followed by loss of ketene (42 mass units) structure 15, containing C-1-C-2-C-3 less a rearranged hydrogen atom from C2, is another possibility. The composition of this ion could be important for confirming the presence of a 3-hydroxyl group. 

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