Benzyl alcohol, o methyl

Benzyl alcohol, o-methyl-, 34, 58 Benzylamine, 35, 91 Benzylamine, 2,3-dimethoxy-N-methyl, 30, 59 N,N,o-trimethyl-, 34, 61... [Pg.85]

N1tro-l-phenylethano1 Benzyl alcohol, o-methyl-m-nitro- (8) Benzenemethano , a-methyl-3-nitro- (9) (5400-78-2)... [Pg.185]

Synonyms Acetic acid, 1-phenylethyl ester Benzenemethanol, a-methyl-, acetate Benzyl alcohol, o-methyl-, acetate Gardenol a-M ethyl benzenemethanol acetate Methylphenylcarbinol acetate Methylphenylcarbinyl acetate s-Phenethyl acetate 1-Phenylethyl acetate o-Phenylethyl acetate... [Pg.2590]

Kinetic and mechanistic investigations on the o-xylene oxidation over V205—Ti02 catalysts were carried out by Vanhove and Blanchard [335, 336] using a flow reactor at 450°C. Possible intermediates like o-methyl-benzyl alcohol, o-xylene-a,a -diol, toluic acid and phthalaldehyde were studied by comparing their oxidation product distribution with that of toluene. Moreover, a competitive oxidation of o-methylbenzyl alcohol and l4C-labelled o-xylene was carried out. The compounds investigated are all very rapidly oxidized, compared with o-xylene, and essentially yield the same products. It is concluded, therefore, that these compounds, or their adsorbed forms may very well be intermediates in the oxidation of o-xylene to phthalic anhydride. The ratio in which the partial oxidation products are formed appears to depend on the nature of the oxidized compounds, i.e. o-methylbenzyl alcohol yields relatively more phthalide, whereas o-xylene-diol produces detectable amounts of phthalan. This... [Pg.215]

SYNS BENZENEMETHANOL, 2-HYDROXY- (9CI) BENZYL ALCOHOL, o-HYDROXY- DIATHESIN a-2-DIHYDROXYTOLUENE 2-HYDROXYBENZENE-METHANOL o-HYDROXYBENZYL ALCOHOL 2-HYDROXA BENZYL ALCOHOL o-(HYDROXYMETH-YL)PHENOL o-METHYLOLPHENOL 2-METHYL-OLPHENOL SAL SALICYL ALCOHOL SAUGENIN SALIGENOL... [Pg.757]

Aniline, acetanilide, benzyl alcohol or methyl benzoate containing a halogen atom in the or /zo-position react with 1 -alkynes in the presence of bis(triphenylphosphine)palladium(II) chloride and copper(I) iodide to give the corresponding o-alkynylbenzenes (e.g. equation 6). Some of the products can be cyclized the aniline derivative 53, for instance, is converted into 2-phenylindole in 99% yield on treatment with a catalytic amount of copper(I) iodide. ... [Pg.293]

Benzyl alcohol o-Anisidine Enanthic acid 2-[2- (2-Methoxyethoxy ) -ethoxy]-ethanol Methyl salicylate... [Pg.369]

Benzyl alcohol formate. See Benzyl formate Benzyl alcohol, p-methyl-. See Cresyl alcohol Benzyl alcohol, a-methyl-, acetate. See o-M ethyl benzyl acetate... [Pg.466]

Methyl-4-(a-hydroxyisopropyl) benzene. See Tri methyl benzyl alcohol 1-Methyl-3-hydroxy-4-isopropyl-6-chlorobenzene. See Chlorothymol o-Methylhydroxylamine hydrochloride CAS 593-56-6 EINECS/ELINCS 209-798-7 UN 1759... [Pg.2641]

Ethyl acetoacetate Methyl succinate Caproic acid 2-Butoxyethanol Benzonitrile Benzyl alcohol o-Cresol... [Pg.155]

Recently, it was found that the addition of benzylamine to 2-(5//)-furano-3-ylmethanesulfonate 280 (X = O—SOaMe) in methanol afforded a 7 1 mixture of the trans- and cw-methyl-A-benzyl-2-hydroxymethylaziridine-2-carboxylates 281 and 282, respectively (00TL3061). Treatment of 281 with benzyl alcohol in the presence of BF3 OEta furnished, after hydrolysis, rac-cw-amino-a-hydroxy-/3-butyrolactone 284 (Scheme 74). [Pg.154]

Alkyl esters are efficiently dealkylated to trimethylsilyl esters with high concentrations of iodotrimethylsilane either in chloroform or sulfolane solutions at 25-80° or without solvent at 100-110°.Hydrolysis of the trimethylsilyl esters serves to release the carboxylic acid. Amines may be recovered from O-methyl, O-ethyl, and O-benzyl carbamates after reaction with iodotrimethylsilane in chloroform or sulfolane at 50—60° and subsequent methanolysis. The conversion of dimethyl, diethyl, and ethylene acetals and ketals to the parent aldehydes and ketones under aprotic conditions has been accomplished with this reagent. The reactions of alcohols (or the corresponding trimethylsilyl ethers) and aldehydes with iodotrimethylsilane give alkyl iodides and a-iodosilyl ethers,respectively. lodomethyl methyl ether is obtained from cleavage of dimethoxymethane with iodotrimethylsilane. [Pg.21]

Benzol hjthiophene, see Naphthalene 1,2,3-Benzotriazin-4 (3/J -one, see Azinnhos-methyl Benzotriazole, see Tetrachloroethylene Benzyl alcohol, see Benzo[a]anthracene, Benzyl butyl phthalate. Benzyl chloride, Permethrin. o-Xylene, m-Xylene, p-Xylene. Toluene 0-Benzyl alcohol, see o-Xylene m-Benzyl alcohol, see m-Xylene p-Benzyl alcohol, see p-Xylene 10-Benzyl-10-hydroanthracen-9-one, see Benzo [ a] anthracene Benzyl hydroperoxide, see Toluene Benzyl nitrate, see Toluene Benzylsuccinic acid, see Toluene... [Pg.1519]

Such regioselectivities are unique and suggest that redox pillared clays may have broad scope and utility as selective, heterogeneous catalysts for liquid phase oxidations. Indeed, V-PILC also catalyzes the oxidation of benzyl alcohol (to a mixture of benzoic acid and benzylbenzoate) whilst a-methyl benzylalcohol is left completely untouched.71 Similarly, p-substituted benzyl alcohols are oxidized whilst o-substituted benzyl alcohols are inert.71... [Pg.51]

U,5-Dihydroxy-2-methoxyphenyl-ethylamine, AP9U 3, U-D i hydroxy-o -[ (methylami no)-methyl]benzyl alcohol, AP92... [Pg.628]

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