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1-Ami no-2-propanol

Ami no-2-propanol a-(1-Ami nopropyl )benzenemet hanol A/-(3-Ami nopropyl )W-met hyl-1,3-propanedi ami ne... [Pg.146]

Ni tram ino-2-methyl-1-propanol Nitrate, 1-NSt nvw.2>nitramino 2-methyi-propane or 1-N i troxy 2- nitr ami no-2,2-dimethyl ethane,... [Pg.233]

Oxazolines are formed directly from the reaction of carboxylic acids with 2-ami-no-2-methyl-l-propanol in refluxing toluene but a two-step procedure involving reaction of 2-amino-2-methyl-l-propanol with an acid chloride followed by treatment of the resultant amide with excess thionyl chloride as a dehydrating agent is generally preferred (Scheme 2.128].2 o 26i Alternatives include reaction of dimethylaziridine with a carboxylic acid in the presence of dicyclohexylcarbo-diimide to form the N-acylaziridine followed by acid-catalysed rearrange-ment or reaction of an orthoester, or an imidate ester, with an amino alcohol as illustrated by the conversion of 129.1 to 1293 [Scheme 2.129). ... [Pg.109]

See other pages where 1-Ami no-2-propanol is mentioned: [Pg.338]    [Pg.331]    [Pg.145]    [Pg.333]    [Pg.591]    [Pg.338]    [Pg.331]    [Pg.145]    [Pg.333]    [Pg.591]    [Pg.375]    [Pg.274]    [Pg.330]    [Pg.397]    [Pg.257]    [Pg.257]    [Pg.277]    [Pg.233]    [Pg.834]    [Pg.116]    [Pg.140]    [Pg.142]    [Pg.265]    [Pg.113]    [Pg.218]    [Pg.328]    [Pg.497]    [Pg.607]    [Pg.674]    [Pg.705]    [Pg.35]    [Pg.136]    [Pg.1311]    [Pg.145]    [Pg.146]    [Pg.330]   


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