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L-Ethoxy-2-propanol

Base-catalyzed epoxide opening is a typical S -2 reaction in which attack of the nucleophile takes place at the less hindered epoxide carbon. For example, 1,2-epoxypropane reacts with ethoxide ion exclusively at the less highly substituted, primary, carbon to give l-ethoxy-2-propanol. [Pg.665]

Electric shaver l-Ethoxy-2-propanol, cyclohexanone, toluene, naphthalene, methylnaphthalenes (isomers), cyclohexanone, C3-C4 benzenes, aliphatic hydrocarbons, BHT 2... [Pg.222]

Oxidations of l-methoxy-2-propanol and l-ethoxy-2-propanol with alkaline ditellura-toargentate(III) are of fractional order in the substrates and subjeet to negative salt effect obs increases with OH but decreases with H4Te06 and a plausible two-electron transfer mechanism has been proposed. ... [Pg.105]

Propylene glycol monobutyl ether) see l-Butoxy-2-propanol (Propylene glycol monoethyl ether) see l-Ethoxy-2-propanol (Propylene glycol monomethyl ether) see l-Methoxy-2-propanol (Propylene glycol monomethyl ether acetate) see l-Methoxy-2-propyl acetate (Propylene glycol monopropyl ether) see l-Propoxy-2-propanol (Propylene glycol monomethyl ether acetate) see l-Methoxy-2-propyl acetate... [Pg.96]

Preparation of Isobutyl Ethyl Ether 5-4. Preparation of l-Ethoxy-2-propanol... [Pg.34]

Trifluoroacetaldehyde, generated from l-ethoxy-2,2,2-trifluoroethanol (4 mmol) by treatment with polyphosphoric acid (PPA), was passed into a toluene solution of (Ry BIN0L-Ti(0-/-Pr)2 (1 mmol) at -78 °C in the presence of 2-propanol (2 mmol) coproduced during the preparation of the catalyst from Ti(0-/-Pr)4 and (i )-binaphthol (BINOL). The resulting hemiacetal was treated with benzoyl chloride, triethylamine and 4-dimethylaminopyridine (DMAP) at -78 °C to afford 2,2,2-trifluoro-l-isopropoxyethyl benzoate (80% ee) in 85% yield. When the esterification was carried out at higher temperatures, % ee of the product considerably decreased due probably to racemization of the intermediate hemiacetal. [Pg.228]

There are five additional five-carbon multifunctional ethers that have been the subject of a single study of their OH reactivity. These include l-ethoxy-2-methoxyethane (Dagaut et al., 1989a), 3-methoxy-1-butanol (Dagaut et al., 1989b), 3-ethoxy-l-propanol (Dagaut et al., 1989b), 2-isopropoxyethanol (Porter et al., 1997), and 1,3-dimethoxypropane (Moriarty et al 2003). For the 1,3-dimethoxypropane relative rate study of Moriarty et al. (2003), the rate coefficient data of Porter et al. (1997) have been used for the reference reaction (OH - - 2-ethoxy ethyl ether, see section ni-C-14 for details). Data are summarized in table III-C-15. In the absence of corroborative measurements, uncertainties of 35% are estimated for these rate coefficients. [Pg.354]

CN ( )-l-[4-[[2-(l-methylethoxy)ethoxy]methyl]phenoxy]-3-[(l-methylethyl)amino]-2-propanol... [Pg.252]

Methan Azido-ethoxy- X/3, 792 2-Propanol 1-Azido- VI/la,l, 420f. [Pg.127]

Kim, Y. Keskinen, K. L Aittamaa, J. Vapor-liquid equilibrium for binary systems 2-propanol + 2-ethoxy-2-methylpiopane and ethyl ethanoate + 2-ethoxy-2-methylpropane at 333 K and 2-propanone + 2-ethoxy-2-methylpropane at 323 K J. Chem. Eng. Dam 2004,49, 1273-1278... [Pg.2279]

Addition of cyclohexyl isocyanide to 4-amino-l-chroma-l,3-dienes ( )-96b-e provides a mild and regiospecific access to l,4-diamino-2-ethoxy naphthalenes 104 [l-NHc-QHn 4-NRR1 = NMe2, (S)-2-hydroxymethyl-pyrrolidinyl, (lf ,25)-2-methylamino-l-phenyl-l-propanol, N-f-BuMe] in... [Pg.199]

Methan Brom-(2-brom-ethoxy)-E14a/3, 35 (l,3-Dioxolan/SOBr2) Propanol 2,3-Dibrom- V/4, 56... [Pg.121]

The aroma compounds studied during the biological ageing of Fino wines belong to different chemical families. The higher alcohols determined were methanol, 2-butanol, 1-propanol, isobutanol, 1-butanol, isoamyl alcohols, 1-pentanol, 3- and 4-methyl-l-pentanol, 1-hexanol, 3-ethoxy-l-propanol, Z-3-hexenol, 1-heptanol, 1-octanol, furfuryl alcohol, 2, 3-butanediol, 1-decanol, benzyl alcohol and phenethyl alcohol. [Pg.99]


See other pages where L-Ethoxy-2-propanol is mentioned: [Pg.268]    [Pg.443]    [Pg.314]    [Pg.268]    [Pg.592]    [Pg.724]    [Pg.204]    [Pg.268]    [Pg.281]    [Pg.268]    [Pg.443]    [Pg.314]    [Pg.268]    [Pg.592]    [Pg.724]    [Pg.204]    [Pg.268]    [Pg.281]    [Pg.1553]    [Pg.500]    [Pg.41]    [Pg.82]    [Pg.100]    [Pg.158]    [Pg.317]    [Pg.28]    [Pg.27]    [Pg.29]    [Pg.29]    [Pg.46]    [Pg.46]    [Pg.94]    [Pg.603]    [Pg.1182]    [Pg.1556]    [Pg.581]    [Pg.381]    [Pg.56]    [Pg.190]   
See also in sourсe #XX -- [ Pg.38 ]




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