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Ethylvinyl ether

We found that LiHBEt3 cleanly reduces the ethylvinyl ether salt 18b in THF to a 6-ethoxyethyl iron complex in 80% yield In contrast, Pt PMe+BHi - in CH2C12 transforms 18b into 1 1 mix-... [Pg.291]

Reaction of ethylvinyl ether (ethoxyethylene) to [Fe(=C=CH2)(CO) (PPh3)( -C5H5)]+ affords the ethoxy(methyl)carbene complex (26) with elimination of acetylene (43) ... [Pg.73]

Dihydro-4-hydroxy-2-(2-methoxy)ethyl-2H-thieno[3,2-e]-l,2-thiazine 1,1-dioxide (4.9 g, 50 18.6 mmol) was converted to the 4-(l-ethoxy)ethoxy-3,4-dihydro-2-(2-methoxy)ethyl-2H-thieno[3,2-e]-l,2-thiazine 1,1-dioxide (6.2 g, 99%) using the reaction with p-toluensulfonic acid and ethylvinyl ether at 0°C in tetrahydrofuran for 2 hrs. [Pg.666]

Homopolymerization and copolymerization with ethylvinyl ether were attempted but no characterization of the obtained polymers has been reported so far. The formed compounds were used as polymeric catalysts in interfacial reactions and showed a significant activity. [Pg.17]

A 0. IM solution of the Step 3 product dissolved in CH2CI2 was charged into a Schlenk tube followed by a CH2CI2 solution of bis(tricyclohexylphosphine)benzylidine ruthenium(IV)dichloride (0.04 eq). The solution was then stirred for 14 hours at ambient temperature. Excess ethylvinyl ether was added, and the solution was stirred while exposed to the atmosphere for 30 minutes. Thereafter the polymer was precipitated into cold diethyl ether, and the product was isolated in 75% yield. [Pg.530]

On the other hand, the Cr-carbene complex reacts with ethylvinyl ether or isobutylvinyl ether, under milder conditions, to give the metathesis product, a-methoxystyreneS ... [Pg.95]

The diphenylalkylidene , W(CO)5CPh2, also undergoes alkylidene exchange reactions when treated with some olefins, including ethylvinyl ether, trans-2-butene, isobutylene and 1-phenyl-l-methoxyethylene, as demonstrated by the organic products of the reaction . The product carbene complex is only isolable when it contains a stabilizing alkoxy substituent ... [Pg.133]

Figure 5. Functional Group Switching problems solved as in Ref. 10. RCHOEE is the ethoxyethyl ether of a secondary alcohol EVE is ethylvinyl ether. Figure 5. Functional Group Switching problems solved as in Ref. 10. RCHOEE is the ethoxyethyl ether of a secondary alcohol EVE is ethylvinyl ether.
ETHYlVINYL ether METHALLYl alcohol TETRAHYDHOFURAN TETRAHYOHOFUHAN, lt2-CPOXY-2-ME PHOPANE 2 2-DlHElHYL PROPANE... [Pg.938]

BHT 2,6-di-tcrt-butyl-4-methylphenol EVE-Li 2-lithio-ethylvinyl ether... [Pg.642]

Ethoxyethoxy) ethoxy] ethene. See Diethylene glycol ethylvinyl ether 2-(2-Ethoxyethoxy) ethyl acetate. See Ethoxydiglycol acetate Ethoxyethoxyethyl acrylate. See 2-(2-Ethoxyethoxy) ethyl acrylate 2-(2-Ethoxyethoxy) ethyl acrylate CAS 7328-17-8 EINECS/ELINCS 230-811-7 Synonyms Acrylic acid, 2-(2-ethoxyethoxy) ethyl ester Carbitol acrylate Diethylene glycol ethyl ether acrylate EEEA EOEOEA Ethoxyethoxyethyl acrylate 2-(2-Ethoxyethoxy) ethyl 2-propenoate Ethoxyethyl acrylate Ethyl Carbitol acrylate 2-Propenoic acid, 2-(2-ethoxyethoxy) ethyl ester Empiricai C9H16O4... [Pg.1678]

Ethoxyethyl 2-(vinyloxy) ethyl ether. See Diethylene glycol ethylvinyl ether Ethoxyformic acid anhydride. See Diethyl... [Pg.1679]

Vinyl ethanoate. See Vinyl acetate Vinyl ether Carbitol. See Diethylene glycol ethylvinyl ether... [Pg.4683]

See other pages where Ethylvinyl ether is mentioned: [Pg.33]    [Pg.420]    [Pg.30]    [Pg.189]    [Pg.364]    [Pg.1055]    [Pg.1537]    [Pg.242]    [Pg.210]    [Pg.212]    [Pg.260]    [Pg.613]    [Pg.322]    [Pg.322]    [Pg.212]    [Pg.213]    [Pg.3369]    [Pg.205]    [Pg.474]    [Pg.531]    [Pg.212]    [Pg.517]    [Pg.3368]    [Pg.71]    [Pg.33]    [Pg.45]    [Pg.45]    [Pg.151]    [Pg.274]    [Pg.1311]    [Pg.5682]    [Pg.6414]   
See also in sourсe #XX -- [ Pg.71 ]

See also in sourсe #XX -- [ Pg.3 , Pg.108 ]



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Vinyls ethylvinyl ether

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