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Chloroethyl ether

Phiorog1iicino1-3,5-dimethyl-1-(2-amino-3-hydroxyhutyryl)ether is characterized by antiarrhythmic activity (176). 2,4-Diacylphloroglucinols were patented as compounds with pronounced anthelmintic activity (177). Phloroglucinol mono- and di-(2-chloroethyl) ethers have antispasmodic or tranquilizing activities (178). 2-(3,5-DiaLkoxyphenoxy)ethylamines have antispasmodic, choloretic, sedative, and vasodilating effects (179). [Pg.385]

Chlorohydrin Process. Ethylene oxide is produced from ethylene chlorohydrin by dehydrochlorination using either sodium or calcium hydroxide (160). The by-products include calcium chloride, dichloroethane, bis(2-chloroethyl) ether, and acetaldehyde. Although the chlorohydrin process appears simpler, its capital costs are higher, largely due to material of constmction considerations (197). [Pg.460]

Chemical Designations - Synonyms Bis(2-chloroethyl) Ether 2,2 -Dichloroethyl Ether Dichlorodiethyl Ether Di-(2-chloroethyl) Ether Chlorex DCEE beta,beta -Dichloroethyl Ether Chemical Formula (ClCHjCH2)20. [Pg.117]

Pedersen s preparation of dibenzo-18-crown-6 involves catechol and bis(2-chloroethyl) ether. In this procedure, sodium hydroxide is used as base and M-butanol as solvent. The reactants are heated overnight and the crude crown is obtained by precipitation from acetone in which it is almost completely insoluble. The yield range specified is 39—48% and is readily realized. The overall preparation is illustrated in Eq. (3.11). [Pg.23]

It is prepd by the interaction of vinyl 2-chloroethyl ether and Petrin in methyl ale catalyzed by a mixt of Hg and Na acetates. [Pg.601]

The oxidation of di-2-chloroethyl ether is first-order with respect to ether, but is autocatalytic and chloride ion is liberated. A hydrogen atom abstraction process, similar to that above, probably takes place, viz. [Pg.383]

C4H8CI2O Bis(2-chloroethyl)ether C4H1QO Diethyl ether... [Pg.473]

Tetrachloroethane Chloroethane Bis(2-chloroethyl)ether 2-Chloroethyl vinyl ether (mixed)... [Pg.385]

HP Sulfur Mustard and Bis(2-chloroethyl) Ether Mixture C03-A001... [Pg.665]

The catalysed -elimination of hydrogen bromide from 2-bromoethyl and 1,2-dibromoethyl sulphides, using 9.1.1 or 9.1.2, provides a convenient route to vinyl and alkynyl sulphides, respectively [17, 18], which, as their sulphoxides or sulphones, have considerable utility as dienophiles. Aryl vinyl ethers (>90%) have been obtained by analogous procedures from 2-chloroethyl ethers [19]. [Pg.393]

See other pages where Chloroethyl ether is mentioned: [Pg.698]    [Pg.465]    [Pg.498]    [Pg.539]    [Pg.584]    [Pg.1088]    [Pg.1199]    [Pg.222]    [Pg.106]    [Pg.109]    [Pg.2211]    [Pg.552]    [Pg.59]    [Pg.65]    [Pg.202]    [Pg.215]    [Pg.698]    [Pg.302]    [Pg.272]    [Pg.1516]    [Pg.2309]    [Pg.304]    [Pg.355]    [Pg.480]    [Pg.748]    [Pg.126]    [Pg.17]    [Pg.683]    [Pg.711]    [Pg.110]    [Pg.734]    [Pg.767]    [Pg.808]    [Pg.853]    [Pg.1357]    [Pg.1468]    [Pg.1570]   
See also in sourсe #XX -- [ Pg.7 ]



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1- Chloroethyl ethyl ether

2- Chloroethyl Chloromethyl Ether

2-Chloroethyl vinyl ether

A-Chloroethyl ethyl ether

Bis(2-chloroethyl) ether

Butyl 1-chloroethyl ether

Chloroethyl methyl ether

Di chloroethyl ether

Dichloromethyl 2-chloroethyl ether

Ether, benzhydryl 2-chloroethyl

Ether, benzhydryl 2-chloroethyl bis

Ether, benzhydryl 2-chloroethyl ethyl

Ether, benzhydryl 2-chloroethyl ethyl ethynyl

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