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Dauben et al., 1952 - Google Patents

The Reaction of α-Haloketones with Bases

Dauben et al., 1952

Document ID
10776330054564313089
Author
Dauben W
Hiskey C
Muhs M
Publication year
Publication venue
Journal of the American Chemical Society

External Links

Snippet

I II displacement product, an amide was isolated and it was shown to be,-dialkyl 9, 10- dihydro-9-anthrylacetamide (II). Such a rearrangement of a-haloketone in the presence of base is wdl-known3· 4 and, indeed, the rearrangement of benzyl chloro-methyl ketone in …
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    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
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    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/587Unsaturated compounds containing a keto groups being part of a ring
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