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Ethoxyacetyl chloride

A9(l 1 )-Estrone methyl ether, 84-85 Etard oxidation, 62 Ethanalation, 73 Ethanolamine, 146 Ether cleavage, 7 Ethoxyacetyl chloride, 137 N-Ethoxycarbonylazepine, 103 N-Ethoxycarbonyl-2-ethoxy-l,3-dihydroquin-oline(EEDQ), 137 Ethoxyketene, 137-138 Ethylamine, 186 Ethyl azidoformate, 138 Ethylbenzene, 328 Ethylbenzenes, 15 Ethyl bromide, 159 Ethyl bromoacetate, 26, 28, 236 Ethyl 4-bromocrotonate, 236 Ethyl bromocyanoacetate, 237 Ethyl chlorodiazoacetate, 222... [Pg.197]

The reagent is generated in situ by dehydrochlorination of ethoxyacetyl chloride with triethylamine at —78°. It appears to be fairly stable at this temperature but slowly polymerizes at room temperature. It is also formed to some extent by photochemical Wolff rearrangement of ethyl diazoacetate. [Pg.274]

See other pages where Ethoxyacetyl chloride is mentioned: [Pg.69]    [Pg.2372]    [Pg.684]    [Pg.421]    [Pg.684]    [Pg.207]    [Pg.69]    [Pg.212]    [Pg.212]    [Pg.69]    [Pg.2372]    [Pg.684]    [Pg.421]    [Pg.684]    [Pg.207]    [Pg.69]    [Pg.212]    [Pg.212]    [Pg.69]   
See also in sourсe #XX -- [ Pg.20 , Pg.212 ]



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