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3-Ethoxyethyl cyanide

Ethoxyethyl cyanide has been prepared by the action of potassium cyanide on /3-ethoxyethyl bromide.1... [Pg.17]

Ethane, 1-bromo-2-ethoxy-, 23, 32 Ethanolamine, 26, 38 Ethanol, 2-isopropylamino-, 26, 38 Ether, anhydrous, 22, 57 Ether, butyl o-nitrophenyl, 25, 9 /3-Ethoxyethyl alcohol, 23, 32 /3-Ethoxyethyl bromide, 23, 32, 33 /3-Ethoxyethyl cyanide, 23, 33 Ethoxymagnesiomalonic ester, 25, 73 2-Ethoxy-1-naphthaldehyde, 20,11 6-Ethoxy-8-nitroquinoline, 27, 52 /3-Ethoxypropionaldehyde acetal,... [Pg.54]

The method has been used for the preparation of dihalides, e.g., 1,9-dichlorononane (93%) unsaturated halides, e.g., 11-undecylenyl chloride (83%) halo ethers, e.g., /3-ethoxyethyl chloride (80%) halo ketones, e.g., desyl chloride (79%) halo esters, e.g, methyl a-chloropropionate (71%) halo cyanides, e.g., phenylchloroacetonitrile (80%) and aminoalkyl halides,An interesting isomerisation has been observed in liberating 2-diethylamino-l-chloropropane from its hydrochloride salt l-diethylamino-2-chloropropane is formed. ... [Pg.51]

Ether, butyl is-nitrophenyl, 25, 9. /3-Ethoxyethyl alcohol, 23, 32 (S-Ethoxyethyl bromide, 23, 32, 33 (3-Ethoxyethvl cyanide, 23, 33 Ethoxymagnesiomalonic ester, 25, 73... [Pg.55]

See other pages where 3-Ethoxyethyl cyanide is mentioned: [Pg.150]    [Pg.43]    [Pg.17]    [Pg.26]    [Pg.34]    [Pg.36]    [Pg.145]   
See also in sourсe #XX -- [ Pg.23 , Pg.33 ]

See also in sourсe #XX -- [ Pg.23 , Pg.33 ]

See also in sourсe #XX -- [ Pg.23 , Pg.33 ]



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1-ethoxyethyl

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