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Ketene, preparation

This Asian species is a major agricultural pest. The pheromone has been proposed to consist of three male-specific compounds, only one of which, (Z)-exo-a-bergamotenal 150, has been reported in the literature [114]. The racemic compound was synthesized starting from farnesoic acid chloride 146 (Scheme 25) [114]. Thus, the vinyl ketene prepared from acid chloride 146 underwent 2+2 cycloaddition to give bicyclic ketone 147. The ketone function was removed by reaction with hydrazine followed by treatment of the resulting hy-... [Pg.82]

Ketene reactivity in intramolecular cycloadditions parallel those in intermolecular reactions in which chloro-, vinyl-, aryl- and alkoxyketenes are more reactive than the alkylketenes. In most instances the ketene is generated by amine dehydrohalogenation of an acid chloride. There are, however, a few examples of ketenes prepared along less conventional routes as by the examples for the formation of 11.150 12,151 and 13.151... [Pg.209]

Thus, [2-1-2] cycloaddition of 2-methylpropene with chloro(2,2,2-trichloroethyl)ketene (prepared in situ from 2,4,4,4-tetrachlorobutanoyl chloride and triethylamine) in cyclohexane yielded 2-chloro-3,3-dimethyl-2-(2,2,2-trichloroethyl)cyclobutanone (70%). This a-chloro-cyclobutanone undergoes a stereoselective cine rearrangement in the presence of triethylamine in refluxing toluene for 20 hours to give cw-(2a,4a)-2-chloro-3,3-dimethyl-4-(2,2,2-tri-chloroethyl)cyclobutanone in 94% yield,which was resolved by means of the diastereomeric salts of their sodium hydrogen sulfite adducts with ( —)- or (- -)-l-phenylethylamine. ... [Pg.1036]

When dimethoxyphosphinyl phenyl ketene, prepared by an Rh-catalyzed Wolff rearrangement of dimethyl l-diazo-2-oxo-2-phenylethylphosphonate, is submitted to the action of (trimethylsi-lyl)diazomethane, it gives rise to the corresponding dimethyl 2-(trimethylsilyl)-l-phenylvinylphos-phonate in reasonable yield (44%, Scheme 2.9). ... [Pg.52]

The initial examples of ketene preparation utihzed efimination reactions from carboxylic acid derivatives in the preparation of diphenylketene (1) by the dehalogenation of 2-chlorodiphenylacetyl chloride with zinc (Eqns (4.1)), and the dehydrochlorination of diphenylacetyl chloride... [Pg.242]

Ketene Prepared from Reagent Yield Refer- ence... [Pg.119]


See other pages where Ketene, preparation is mentioned: [Pg.444]    [Pg.125]    [Pg.154]    [Pg.125]    [Pg.122]    [Pg.219]    [Pg.408]    [Pg.307]    [Pg.174]    [Pg.120]    [Pg.202]    [Pg.1828]   
See also in sourсe #XX -- [ Pg.667 ]

See also in sourсe #XX -- [ Pg.667 ]




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Acetic acid, iododifluorosilyl ketene acetal preparation

Ketene acetals preparation

Ketene dimers preparation

Ketene dithioacetal derivative preparation

Ketene thioacetals preparation

Ketene, commercial preparations

Ketenes, carbenes from preparation

Ketenes, preparation

Ketenes, preparation from 0-lactones

Ketenes, preparation from acids

Ketenes, preparation from acyl halides

Ketenes, preparation from anhydrides

Ketenes, preparation from diazoketones

Ketenes, preparation from dimers

Ketenes, preparation from esters

Ketenes, preparation from ketones

Ketenes, preparation tables

Silyl Enol Ethers and Ketene Acetals Preparation

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