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N-caproate

Small quantities of esters (in the above example n-hexyl n-caproate CH3(CHj)3COO(CH2)jCH3) are simultaneously formed. This is an excellent method for the preparation of aldehydes. [Pg.318]

If tile high boiling residue is transferred to a small Claisen flask and distilled, some n-hexj l alcohol passes over first, followed by n-hexyl n-caproate (2 g.) at 240-250° (mainly 245°). [Pg.322]

It is essential to remove the alcohol completely, otherwise some ethyl n-caproate, b.p. 168°, is formed which will contaminate the final product. [Pg.486]

See other pages where N-caproate is mentioned: [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.318]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.537]    [Pg.537]    [Pg.241]    [Pg.301]    [Pg.145]    [Pg.360]    [Pg.360]    [Pg.596]    [Pg.273]    [Pg.318]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.397]    [Pg.254]    [Pg.255]   
See also in sourсe #XX -- [ Pg.221 ]



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Caproate

Caproates

Ethyl n-caproate

Methyl n-caproate

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