3- methyl-furfuryl alcohol

Another example of an enzymatic one-pot multiple Diels-Alder reaction is illustrated in Table 4.20 [83]. Racemic furfuryl alcohols 130 in the presence of ethoxy vinyl methyl fumarate 131 and enzyme TOYOBO-LIP undergo enzymatic acylation followed by kinetic enzymatic resolution to give the acyl derivatives 132 which then affords the adducts 133 and 134 by intramolecular Diels-Alder reaction 3-methyl-furfuryl alcohol 130 (R = Me) in acetone gives the best results. [Pg.182]

In this context, it must be noted that it would be unreasonable to use purified FU to make furfuryl alcohol as essentially all of the furfuryl alcohol is used to make foundry resins, where any 5-methyl furfural, hydrogenated to 5-methyl furfuryl alcohol, does not matter at all, and may in fact be beneficial. Thus, only FU used as FU, for instance in extraction processes, is a candidate for the given purification process. For most FU manufacturers, this is only 35 percent of their production. [Pg.85]

Under acidic conditions, furfuryl alcohol polymerizes to black polymers, which eventually become crosslinked and insoluble in the reaction medium. The reaction can be very violent and extreme care must be taken when furfuryl alcohol is mixed with any strong Lewis acid or Brn nstad acid. Copolymer resins are formed with phenoHc compounds, formaldehyde and/or other aldehydes. In dilute aqueous acid, the predominant reaction is a ring opening hydrolysis to form levulinic acid [123-76-2] (52). In acidic alcohoHc media, levulinic esters are formed. The mechanism for this unusual reaction in which the hydroxymethyl group of furfuryl alcohol is converted to the terminal methyl group of levulinic acid has recendy been elucidated (53). [Pg.79]

In acidic solution, the degradation results in the formation of furfural, furfuryl alcohol, 2-furoic acid, 3-hydroxyfurfural, furoin, 2-methyl-3,8-dihydroxychroman, ethylglyoxal, and several condensation products (36). Many metals, especially copper, cataly2e the oxidation of L-ascorbic acid. Oxalic acid and copper form a chelate complex which prevents the ascorbic acid-copper-complex formation and therefore oxalic acid inhibits effectively the oxidation of L-ascorbic acid. L-Ascorbic acid can also be stabilized with metaphosphoric acid, amino acids, 8-hydroxyquinoline, glycols, sugars, and trichloracetic acid (38). Another catalytic reaction which accounts for loss of L-ascorbic acid occurs with enzymes, eg, L-ascorbic acid oxidase, a copper protein-containing enzyme. [Pg.13]

Ethylene oxide Propylene oxide Butyl vinyl ether Ethyl vinyl ether Methyl vinyl ether Divinyt ether Furfuryl alcohol I.A-Dioxan Furan... [Pg.262]

As an example, a convenient preparation of methyl (E) and (Z)-4,4-dimethoxybutenoa-tes can be performed by anodic oxidation of furfuryl alcohol, furfural or furoic acid via a dimethoxylated dihydrofuran intermediate (Scheme 132) [157]. [Pg.382]

AI3-00040, see Cyclohexanol AI3-00041, see Cyclohexanone AI3-00045, see Diacetone alcohol AI3-00046, see Isophorone AI3-00050, see 1,4-Dichlorobenzene AI3-00052, see Trichloroethylene AI3-00053, see 1,2-Dichlorobenzene AI3-00054, see Acrylonitrile AI3-00072, see Hydroquinone AI3-00075, see p-Chloro-rrr-cresol AI3-00078, see 2,4-Dichlorophenol AI3-00085, see 1-Naphthylamine AI3-00100, see Nitroethane AI3-00105, see Anthracene AI3-00109, see 2-Nitropropane AI3-00111, see Nitromethane AI3-00118, see ferf-Butylbenzene AI3-00119, see Butylbenzene AI3-00121, see sec-Butylbenzene AI3-00124, see 4-Aminobiphenyl AI3-00128, see Acenaphthene AI3-00134, see Pentachlorophenol AI3-00137, see 2-Methylphenol AI3-00140, see Benzidine AI3-00142, see 2,4,6-Trichlorophenol AI3-00150, see 4-Methylphenol AI3-00154, see 4,6-Dinitro-o-cresol AI3-00262, see Dimethyl phthalate AI3-00278, see Naphthalene AI3-00283, see Di-rj-butyl phthalate AI3-00327, see Acetonitrile AI3-00329, see Diethyl phthalate AI3-00399, see Tributyl phosphate AI3-00404, see Ethyl acetate AI3-00405, see 1-Butanol AI3-00406, see Butyl acetate AI3-00407, see Ethyl formate AI3-00408, see Methyl formate AI3-00409, see Methanol AI3-00520, see Tri-ocresyl phosphate AI3-00576, see Isoamyl acetate AI3-00633, see Hexachloroethane AI3-00635, see 4-Nitrobiphenyl AI3-00698, see IV-Nitrosodiphenylamine AI3-00710, see p-Phenylenediamine AI3-00749, see Phenyl ether AI3-00790, see Phenanthrene AI3-00808, see Benzene AI3-00867, see Chrysene AI3-00987, see Thiram AI3-01021, see 4-Chlorophenyl phenyl ether AI3-01055, see 1.4-Dioxane AI3-01171, see Furfuryl alcohol AI3-01229, see 4-Methyl-2-pentanone AI3-01230, see 2-Heptanone AI3-01231, see Morpholine AI3-01236, see 2-Ethoxyethanol AI3-01238, see Acetone AI3-01239, see Nitrobenzene AI3-01240, see I idine AI3-01256, see Decahydronaphthalene AI3-01288, see ferf-Butyl alcohol AI3-01445, see Bis(2-chloroethoxy)methane AI3-01501, see 2,4-Toluene diisocyanate AI3-01506, see p,p -DDT AI3-01535, see 2,4-Dinitrophenol AI3-01537, see 2-Chloronaphthalene... [Pg.1457]

Hydroxymethylfuran, see Furfuryl alcohol 2-Hydroxymethyloxiran, see Glycidol 4-Hydroxy-4-methylpentanone-2, see Diacetone alcohol 4-Hydroxy-4-methylpentan-2-one, see Diacetone alcohol 4-Hydroxy-4-methyl-2-pentanone, see Diacetone alcohol... [Pg.1491]

Reduction of the alcohol group to produce 2-methyl furan can be achieved using a commercial Cu/Zn/Al/Ca/Na catalyst with the atomic ratio 59 33 6 1 1. This catalyst was found to achieve 99.7% conversion with 87.0% selectivity to 2-methyl fural at 250 °C. Hydrogenation from furfuryl alcohol yields a slightly higher selectivity of 92.7% at 98.1% conversion under similar conditions. [Pg.42]

Furfural, 5-methoxy-methyl Cured Lf Furfuryl alcohol Cured Lf ... [Pg.278]

The sequence with oxazole 73 also proves to be applicable to systems in which the double bond of the allylic alcohol fragment is incorporated into a heteroaromatic ring, such as in furfuryl alcohol (77a) and thiophene-2-methanol (77b).28 After hydrolysis of the oxazolone ring with water, V-benzoyl-3,3,3-trifluoro-2-(2-methyl-3-furyl)alanine (79a) and /V-benzoyl-3,3,3-trifluoro-2-(2-melhyl-3-thienyl)alanine (79b) are obtained. The 2-methylene helerocyclcs 78 originally formed in the Claisen rearrangement undergo rearomatizalion under the reaction conditions. [Pg.212]

Fio, 1.—Curves for Light-absorption in the Dische Test (o) 2-Desoxy-D-ribose (61) D-Arabinal (i2) L-Arabinal (c) Furfuryl alcohol (d) w-Methoxylevulinaldehyde Dimethyl Acetal (e) Sodium Thymonucleate (/) Methyl 2-desoxy-/3-n-ribopyrano-side (g) Methyl 3,4-Dimethyl-2-desoxy-/3-L-ribopyranoside. [Pg.57]

Similar irradiation of 2-CN with furfuryl alcohol and furfuryl methyl ether gives the corresponding caged products in almost the same ratios (2 1). However, the photoreaction of 3-furylmethanol to 2-CN gives two isomeric cage products in a 5 1 ratio. [Pg.163]

Methyl-2-furfuryl alcohol 2,3-Dihydro-3,5-dihydroxy-6-methyl- 9.0... [Pg.318]

The odor of isomaltol is described as sweet, but with a burnt sugar and fruity character (H) 2-Acetylfuran and 2-hydroxyacetylfuran impart burnt sweetish flavors. Furfuryl alcohol and 5-methyl-2-furaldehyde have sweet caramellic flavors (31). The major formation route to most furans in heated-abused citrus products has been postulated as acid-catalyzed enolizations and dehydrations of sugars (38). Furans, such as 2-hydroxyacetylfuran and isomaltol... [Pg.338]

FurfuraI-5-carboxylic acid, IV, 332 Furfuryl alcohol, a-methyl-4-hydroxytet-rahydro-, IV, 300... [Pg.348]

Fully Hydrogenated Rapeseed Oil, 44 Furfuryl Alcohol, 74, 100 2-I ui yl Methyl Ketone, 74, 100 Fusel Oil, Refined, 76... [Pg.113]

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