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Ethyl chlorosulfonate

In the presence of Eriedel-Crafts catalysts, gaseous ethyl chloride reacts with ben2ene at about 25°C to give ethylben2ene, three diethylben2enes, and other more complex compounds (12) (see Xylenes and ethylbenzene). Aromatic compounds can generally be ethylated by ethyl chloride in the presence of anhydrous aluminum chloride (see Eriedel-Crafts REACTIONS). Ethyl chloride combines directly with sulfur trioxide to give ethyl chlorosulfonate,... [Pg.2]

No. 13 (French WWI Shell) Ethyl Chlorosulfonate (75%) and Stannic Chloride (25%) Mixture ... [Pg.682]

This product hydrolyzes very slowly however, it is rapidly destroyed by sodium hydroxide. It is miscible with alcohol and ether with no apparent reaction. 2-Chloroethyl chlorosulfonate is more stable than ethyl chlorosulfonate. It is quite stable thermally no polymerization is apparent. Upon long standing, decomposition occurs with the evolution of hydrogen chloride as evidenced by darkening of the liquid. [Pg.87]

Ethyl bromacetate Ethyl chlorosulfonate Ethyldichlorarsine Ethyl iodoacetate Hexachlorethane HC mixture... [Pg.58]

Cyclic esters s. 18,143 also with ethyl chlorosulfonate s. D. Lipkin and T. Laylotf, J. Chem. Eng. Data 15, 450 (1970)... [Pg.338]

Ethyl chlorosulfinate Ethyl chlorosulfonate S-Ethyl chlorolhiotormate... [Pg.386]

See other pages where Ethyl chlorosulfonate is mentioned: [Pg.278]    [Pg.657]    [Pg.414]    [Pg.523]    [Pg.65]    [Pg.363]    [Pg.355]    [Pg.64]    [Pg.312]    [Pg.397]    [Pg.398]    [Pg.115]    [Pg.385]    [Pg.396]    [Pg.55]   
See also in sourсe #XX -- [ Pg.278 ]

See also in sourсe #XX -- [ Pg.54 , Pg.55 ]



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Chlorosulfonated

Chlorosulfonation

Sulfuric acid, fuming ethyl chlorosulfonate

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