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Acetals alkyl

Diisobutylaluminium benzeneteUurolate, generated in situ from diphenyl ditelluride and diisobutylaluminium (DIBAL), reacts with acetals, alkyl sulphonates and oxiranes, giving the expected tellurides in high yields. ... [Pg.28]

Unlike typical aldehydes, 1 mol of glucose reacts with only 1 mol of ROH in dry HCI to give two isomeric acetals (alkyl glycosides). See Problem 15.35. [Pg.499]

PET degrades thermally during processing at 280-300 °C. The chain scission is catalyzed by transesterification catalysts (zinc, manganese or cobalt acetates, alkyl titan-ates). PET is stabilized by tributyl phosphate (46) or triphenyl phosphate (47), considered as heat stabilizers and metal deactivators (Karayannidis et al., 1998). [Pg.64]

In the alkaline medium, the reagent is postulated to be hydroxymethylamine or methylenc-bis-amine, - - although the participation of the N,0-acetal (Alkyl-O—CH2— N<), when the reaction is carried out in alcoholic solvents, cannot be excluded, and relevant amounts of methyleneimmonium cation are observed. The C-NMR measurements indicate that the methylolamine concentration is maximum when the molar ratio amine/aldehyde is ca. 1, whereas the formation of methylene-bis-amine is favored when this ratio increases. [Pg.17]

The reaction of chloromethyl methyl ether (MOM-Cl, a carcinogen) with an alkoxide or with an alcohol in the presence of /-Pr2NEt (Hiinig s base) furnishes the corresponding formaldehyde acetal. Alkylation of 3°-alcohols requires the more reactive MOM-I, derived from MOM-Cl and Nal in the presence of /-ProNEt. ... [Pg.66]

Linear polyurethanes dissolve in various solvents such as ketones (methyl ethyl ketone, cyclohexanone, etc.), acetate alkyl esters (methyl acetate, butyl acetate), THF, dimethylformamide, methylene chloride, trichloroethane, etc. [Pg.546]

Aliphatic pseudo bases, e.g., 19 20 (R = R = R" = Me), are much less stable they are colorless water-soluble liquids which resinify rapidly in the air. For their preparation, barium carbonate can be replaced by sodium carbonate, sodium hydrogen carbonate, or sodium acetate. Alkyl-aryl derivatives are also unstable, because in these cases anhydro bases are also formed and the possibilities for aldol condensations or polymerizations are greatly increased. [Pg.269]

R = acetal, alkyl, cyclic-alkyl, silyl, silylether R = heteroaiyl, alkyl, halo, ester... [Pg.11]

R = CF3SO2-, acetate, alkyl, acetyl Fig. 3.9. Derivatization of aromatic position 5 of phenyl tetrahydrophthalimide. [Pg.160]

Heat-shrinkable film comprised single-site catalyzed Babrowicz et al. (1994) copolymer of ethylene and a 3-8C alpha-olefin, LLDPE with p > 9(X) kg m blended with another polymer of ethylene and a 3-8C alpha-olefin and a second comonomer [e.g., vinyl acetate, alkyl acrylate, CO, butadiene, styrene, acrylic acid, and a metal salt of an acrylic acid], or an alpha-olefin homopol3uner. The films had improved shrinkability, impact resistance, and optical properties as compared to prior art and were used in packaging... [Pg.1684]

Vinyl acetate Alkyl acrylate Single Tg FTIR I had an alkyl group of methyl, ethyl, or butyl Princi et al. (2009)... [Pg.2032]


See other pages where Acetals alkyl is mentioned: [Pg.269]    [Pg.67]    [Pg.333]    [Pg.29]    [Pg.2356]    [Pg.2548]    [Pg.2548]    [Pg.2549]    [Pg.265]    [Pg.192]    [Pg.2356]    [Pg.2548]    [Pg.2548]    [Pg.2549]    [Pg.116]    [Pg.1296]    [Pg.2584]    [Pg.814]    [Pg.308]    [Pg.60]    [Pg.157]    [Pg.157]    [Pg.158]    [Pg.392]    [Pg.303]    [Pg.1620]    [Pg.117]   
See also in sourсe #XX -- [ Pg.103 ]




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1- Substituted 2-propenyl acetate, allylic alkylations

2.7- Octadienyl acetates, 4-alkyl-4-hydroxycyclization

2.7- Octadienyl acetates, 4-alkyl-4-hydroxycyclization palladium-ene reaction

Acetals alkyl groups

Acetic alkyl phosphines

Acetic formic anhydride alkylation reactions

Aceto acetic acid Alkyl derivatives

Alkyl acetates

Alkyl acetates

Alkyl acetates, elimination reactions

Alkyl ammonium acetate

Alkyl glucosides/glycosides acetals

Alkyl mercury acetate

Alkyl methoxy acetates

Alkyl nitronates nitroso acetal functionalization

Alkylating reagents dialkyl acetals

Alkylation Baylis-Hillman acetates

Alkylation of acetals

Alkylation of chiral acetals

Alkylation stannylene acetals

Alkylations indoles, palladium®) acetate

Asymmetric allylic alkylations -1,3-diphenylprop-2-enyl acetate

Baylis-Hillman acetates alkylation with

Cyclic acetates, asymmetric allylic alkylations

Cyclic allylic acetates, alkylation

Dibutylstannylene acetals alkylation

Diphenylallyl acetate, asymmetric allylic alkylation

Dithioacetals, alkylation from acetals

Formyl acetate, alkyl

Ketene alkyl silyl acetals, reactions

Ketene alkyl trialkylsilyl acetals or ketals

Methylketene alkyl trialkylsilyl acetals

N-Alkylation acetals

Nitroso acetals alkyl nitronates

Palladium acetate alkylations

Silver acetate alkylation with

Silyl alkyl acetals

Silyl ketene acetals alkylation

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