Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Ethyl a-naphthoate

In a 1-5-litre three-necked flask prepare a solution of a-naphthyl magnesium bromide from 12 2 g. of magnesium turnings as detailed under [Pg.785]

This reaction has been used infrequently for the preparation of esters. Simultaneous reaction of the Grignard reagent with the ester formed leads to tertiary alcohols (method 91). However, if the organometallic reagent is relatively unreactive or if it is added to an excess of ethyl car-bonate, esters may be isolated. A typical example is the preparation of ethyl a-naphthoate (73%). ... [Pg.700]

See other pages where Ethyl a-naphthoate is mentioned: [Pg.781] [Pg.785] [Pg.785] [Pg.789] [Pg.785] [Pg.785] [Pg.789] [Pg.781] [Pg.785] [Pg.785] [Pg.789] [Pg.1175] [Pg.256] [Pg.785] [Pg.785] [Pg.789] [Pg.781] [Pg.785] [Pg.785] [Pg.789]

See also in sourсe #XX -- [ Pg.781 , Pg.785 ]

See also in sourсe #XX -- [ Pg.781 , Pg.785 ]

See also in sourсe #XX -- [ Pg.424 ]

See also in sourсe #XX -- [ Pg.781 , Pg.785 ]

See also in sourсe #XX -- [ Pg.781 , Pg.785 ]

SEARCH

2-Naphthoate

Ethyl-2-naphthoate

Naphthoates