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Amides from alcohols

Hydrolysis may be effected with 10-20 per cent, sodium hydroxide solution (see p-Tolunitrile and Benzonitrile in Section IV,66) or with 10 per cent, methyl alcoholic sodium hydroxide. For diflScult cases, e.g., a.-Naphthoniirile (Section IV,163), a mixture of 50 per cent, sulphuric acid and glacial acetic acid may be used. In alkahne hydrolysis the boiling is continued until no more ammonia is evolved. In acid hydro-lysis 2-3 hours boiling is usually sufficient the reaction product is poured into water, and the organic acid is separated from any unchanged nitrile or from amide by means of sodium carbonate solution. The resulting acid is identified as detailed in Section IV,175. [Pg.805]

Acid chloride, alcohols from, 804 alcoholysis of, 802-803 amides from, 803-804 amines from, 933-935 amjnolysis of, 803-804 carboxylic acids from, 802 electrostatic potential map of, 791... [Pg.1281]

The most representative non-ionic surfactants are the alkyl (alcohol) ethoxylates. These are adducts of a long-chain alcohol (12—18) with a variable number of EO units (3-11). Other non-ionic surfactants are derived from carbohydrates (glucoside and glucamide derivatives), organosilicones, fatty alcohols, and amides. Products in this category are as follows (compare also Table 1.2) ... [Pg.35]

The reason why the carbonyl group in -santonin remained intact may be that, after the reduction of the less hindered double bond, the ketone was enolized by lithium amide and was thus protected from further reduction. Indeed, treatment of ethyl l-methyl-2-cyclopentanone-l-carboxylate with lithium diisopropylamide in tetrahydrofuran at — 78° enolized the ketone and prevented its reduction with lithium aluminum hydride and with diisobutyl-alane (DIBAL ). Reduction by these two reagents in tetrahydrofuran at — 78° to —40° or —78° to —20°, respectively, afforded keto alcohols from several keto esters in 46-95% yields. Ketones whose enols are unstable failed to give keto alcohols [1092]. [Pg.162]

Alkylation with aldehyde 107 Alkylation, enantioselective 165 Alkylation, intramolecular 134,167 Enantioselective Mannich 151 From alcohol 26,41,86,176 From amide 11, 109,163 Halogenation, enantioselective 158... [Pg.112]


See other pages where Amides from alcohols is mentioned: [Pg.36]    [Pg.441]    [Pg.443]    [Pg.445]    [Pg.447]    [Pg.449]    [Pg.36]    [Pg.36]    [Pg.237]    [Pg.239]    [Pg.241]    [Pg.243]    [Pg.245]    [Pg.451]    [Pg.85]    [Pg.85]    [Pg.36]    [Pg.441]    [Pg.443]    [Pg.445]    [Pg.447]    [Pg.449]    [Pg.36]    [Pg.36]    [Pg.237]    [Pg.239]    [Pg.241]    [Pg.243]    [Pg.245]    [Pg.451]    [Pg.85]    [Pg.85]    [Pg.395]    [Pg.111]    [Pg.67]    [Pg.1290]    [Pg.1297]    [Pg.145]    [Pg.618]    [Pg.403]    [Pg.449]    [Pg.125]    [Pg.103]    [Pg.44]    [Pg.95]    [Pg.416]    [Pg.318]    [Pg.263]    [Pg.615]    [Pg.738]    [Pg.59]   
See also in sourсe #XX -- [ Pg.1644 ]

See also in sourсe #XX -- [ Pg.410 ]




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Acid anhydride, amides from reaction with alcohols

Alcohols amidation

Amidations alcohols

Amides from alcohols and amines

Amides from allylic alcohols

From amides

Hydroxy-amides, from addition amino-alcohols

Synthesis of Amides from Alcohols and Amines

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