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1.1- dihalo-1-alkene alkanal

The method of greatest applicability is the reaction of alkali metal phosphides with dihalo-alkanes, -alkenes, etc. (equation 4). Generally this reaction proceeds well and in high yield excess dihaloalkane should be avoided as this leads to the production of phosphonium salts which can contaminate the product. [Pg.992]

Analogous sulfur compounds are also prepared. 1,2-Dihalo compounds lead to the formation of alkenes (see above), as do l-halo-2-X-substituted alkanes (X = NRjOR, SR, etc.). In the aromatic series 2-heterosubstituted reagents can be stable , for elimination would lead to highly strained arynes. Similarly, the elimination reaction may be difficult when allenes ... [Pg.405]


See other pages where 1.1- dihalo-1-alkene alkanal is mentioned: [Pg.2380]    [Pg.2380]    [Pg.2384]    [Pg.2384]    [Pg.1214]    [Pg.2508]    [Pg.2381]    [Pg.2533]    [Pg.177]    [Pg.2153]    [Pg.2384]    [Pg.2384]    [Pg.2526]    [Pg.1214]    [Pg.1214]    [Pg.2507]    [Pg.2507]    [Pg.2507]   
See also in sourсe #XX -- [ Pg.581 , Pg.582 , Pg.726 , Pg.727 , Pg.1468 ]




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2- -2-alkenal alkanal

4.4- dihalo-2- -3- alkanal

Alkanes dihalo

Dihalo

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