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Dichlorodiethyl ether

Solvent Treatment. Solvent processes can be divided into two main categories, solvent extraction and solvent dewaxing. The solvent used in the extraction processes include propane and cresyHc acid, 2,2 -dichlorodiethyl ether, phenol (qv), furfural, sulfur dioxide, benzene, and nitrobenzene. In the dewaxing process (28), the principal solvents are benzene, methyl ethyl ketone, methyl isobutyl ketone, propane, petroleum naphtha, ethylene dichloride, methylene chloride, sulfur dioxide, and iV-methylpyrroHdinone. [Pg.208]

Quite recently, Ciampolini and coworkers have reported the synthesis of two isomeric mked oxygen-phosphorus macrocycles and the crystal structures of their cobalt complexes. Synthesis of macrocycle 27 was accomplished by condensation of 1,2-bis-(phenylphosphino)ethane dianion with 2,2 -dichlorodiethyl ether in THE. The two isomers of 27 were isolated in 1.5% and 2% yield. The synthesis is formulated in Eq. (6.17), below. [Pg.275]

Synonyms AI3-04504 BCEE Bis(P-chloroethyl) ether BRN 0605317 Caswell No. 309 Chlorex l-Chloro-2-(P chloroethoxy)ethane Chloroethyl ether 2-Chloroethyl ether (P-Chloro-ethyl) ether CCRIS 88 DCEE Dichlorodiethyl ether 2,2 -Dichlorodiethyl ether p,P -Dichlorodi-ethyl ether Dichloroether Dichloroethyl ether a,a -Dichloroethyl ether Di(p-chloroethyl) ether Di(2-chloroethyl) ether sj/n-Dichloroethyl ether 2,2 -Dichloroethyl ether Dichloroethyl oxide l,5-Dichloro-3-oxapentane EINECS 203-870-1 ENT 4504 EPA pesticide chemical code 029501 NSC 406647 l,l -Oxybis(2-chloroethane) RCRA waste number U025 UN 1916. [Pg.176]

Dichloro-2,2-di(p-chlorophenyl)ethane, see p.p -DDD Dichlorodiethyl ether, see Bis(2-chloroethyl) ether 2,2 -Dichlorodiethyl ether, see Bis(2-chloroethyl ether) p,p -Dichlorodiethyl ether, see Bis(2-chloroethyl ether) Dichlorodiethyl formal, see Bis(2-chloroethoxy)methane Di-2-chloroethyl acetal, see Bis(2-chloroethoxy)methane Di-2-chloroethyl formal, see Bis(2-chloroethoxy)methane... [Pg.1475]

Many unsaturated chloro- and bromo-hydrocarbons and many polychloro and polybromo compounds decompose by radical-chain mechanisms, but only the chloro compounds have been studied in reasonable detail, presumably owing to the complex nature of the chain reactions in the case of the bromo compounds. Other examples of compounds which undergo radical-chain decompositions are 2,2-dichlorodiethyl ether oxalyl chloride alkyl hypochlorites alkyl peroxychloroformates and alkyl chloro-sulphites in the gas phase ... [Pg.182]

Derivation Reaction of amixture of sodium hydroxide and triethanolamine with 2,2 -dichlorodiethyl ether. [Pg.281]

Iron(III) is extracted from hydrochloric acid media by diethyl ether, DIPE, 2,2 -dichlorodiethyl ether, and MIBK. For MIBK, the optimum concentration is 6-7 M HCl, while in the case of DIPE it is 7-8 M HC1. During the extraction of the iron(III) chloride complex, Ga, Tl(III), Au(III), Ge, As, Sb, and Mo are also extracted. Iron(III) can also be extracted from HCl medium with TBP, TOPO, or TO A in chloroform [1]. Iron(III) has been extracted from bromide media with TBP [2] and from citrate media with Aliquat 336S [3]. Crown ethers in CHCI3 have been also recommended for extraction of Fe(III) [4]. [Pg.226]

DICHLOR-BENZOL (German) (106-46-7), o-DICHLORBENZOL (German) (95-50-1), p-DICHLORBENZOL (German) (106-46-7) see dichlorobenzenes. 2,2 -DICHLOR-DIAETHYLAETHER (German) (111-44-4) see dichlorodiethyl ether or 2,2 -dichlorodiethyl ether. [Pg.322]

DICHLORODIETHYL ETHER or 2,2 -DICHLORODIETHYL ETHER (111-44-4) C4HgCl20 Combustible andperoxidizable liquid. Forms explosive mixture with air [explosion limits in air (vol %) 2.7 to uel unknown flash point 131°F/55°C ... [Pg.326]

I Synonyms/Trade Names bis(2-Chloroethyl)ether 2,2 -Dichlorodiethyl ether, 2,2 -Dichloroethyl ether... [Pg.100]

The fully saturated monocyclic 1,4,5-oxadiazepines of type (91) can be prepared by the reaction of 2,2 -dichlorodiethyl ether with various substituted hydrazines (90) (Equation (2)) <75M1 915-01, 79MI915-01, 81M1915-01>. [Pg.342]

Dichlorodiethyl ether p,p-Dichlorodiethyl ether. See sym-Dichloroethyl ether Dichlorodiethyl formal. See Bis (2-chloroethoxy) methane Dichlorodiethylsilane. See Diethyidichlorosilane Dichlorodifluoromethane CAS 75-71-8 EINECS/ELINCS 200-893-9 UN 1028 (DOT) INS940... [Pg.1260]

Synonyms Bis (2-chloroethyl) ether Bis (P-chloroethyl) ether 1-Chloro-2-(P-chloroethoxy) ethane Chloroethyl ether DCEE 2,2 -Dichlorethyl ether 2,2 -Dichlorodiethyl ether p,p-Dichlorodiethyl ether Dichloroether Dichloroethyl ether... [Pg.1265]

In some situations, dialkylation is desired and there are several useful applications of this technique reported. 1,4-Dibromobutane [24] and 1,5-dibromopentane [24] alkylate phenylacetonitrile according to equation 10.12 to give 1-cyano-l-phenyl-cyclopentane or -hexane in 88% and 40% yields respectively [24]. Alkylation with 2,2 -dichlorodiethyl ether affords the oxygen containing six-membered ring in almost... [Pg.140]

Dichloroacetone Dichloroacetyl chloride 2,2 -Dichlorodiethyl ether Dichlorodifluoromethane... [Pg.162]


See other pages where Dichlorodiethyl ether is mentioned: [Pg.24]    [Pg.1576]    [Pg.191]    [Pg.322]    [Pg.908]    [Pg.805]    [Pg.179]    [Pg.404]    [Pg.405]    [Pg.26]    [Pg.229]    [Pg.398]    [Pg.1451]    [Pg.651]    [Pg.282]    [Pg.25]    [Pg.864]    [Pg.28]    [Pg.756]    [Pg.315]    [Pg.761]    [Pg.457]    [Pg.595]    [Pg.602]    [Pg.613]    [Pg.156]    [Pg.327]    [Pg.759]    [Pg.999]   
See also in sourсe #XX -- [ Pg.24 , Pg.275 ]




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