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Dichloroethyl hydroperoxide

The crude products of ozonolysis at — 30°C of the chloroalkene tended to decompose explosively on warming to ambient temperature, particularly in absence of solvents. The products included the individually explosive compounds acetyl 1,1,-dichloroethyl peroxide, 3,6-dichloro-3,6-dimethyl-2,3,5,6-tetraoxane and diacetyl peroxide [1], Ozonolysis in ethyl formate saturated with hydrogen chloride gives a high yield of 1,1-dichloroethyl hydroperoxide as a further unstable intermediate product [2],... [Pg.1869]

Chlorophenyl)-l,l-dimethylethyl hydroperoxide, 3018 2-Cyclohexenyl hydroperoxide, 2435 1,1-Dichloroethyl hydroperoxide, 0794 3,5-Dimethyl-3-hexyl hydroperoxide, 3075 Ethyl hydroperoxide, 0925... [Pg.40]


See other pages where Dichloroethyl hydroperoxide is mentioned: [Pg.302]    [Pg.685]    [Pg.1454]    [Pg.685]    [Pg.335]    [Pg.2076]    [Pg.295]    [Pg.295]    [Pg.1990]    [Pg.302]    [Pg.685]    [Pg.1454]    [Pg.685]    [Pg.335]    [Pg.2076]    [Pg.295]    [Pg.413]    [Pg.295]    [Pg.1990]    [Pg.267]    [Pg.174]   
See also in sourсe #XX -- [ Pg.685 , Pg.686 ]




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