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Dimethyl ethyl carbinol

Dimethyl ethyl carbinol (2-methy 1-2-butanol or amyl alcohol), CH3CHjCOH(CH3).2. From ethyl propionate and methyl magnesium iodide. Collect the tertiary alcohol at 100-102°. [Pg.260]

Dimethyldiphenyl, 596, 616 Dimethyl ethyl carbinol, 260 Dimethyl ethynyl carbinol, 467, 468 P P - Dimethylglutaric acid, 876 Dimethylglyoxime, 952... [Pg.1173]

Synonyms Amylene hydrate Dimethyl ethyl carbinol 2-Methyl-2-butanol 2-Methyl butanol-2 3-Methylbutan-3-ol t-Pentanol t-Pentyl alcohol... [Pg.292]

Dimethylethyl) benzoic acid, polymer with 1,2-benzenedicarboxylic anhydride and 2-methyl-2-hydroxymethyl-1,3-propanediol. See Butyl benzoic acid/phthalic anhydride/trimethylolethane copolymer Dimethyl ethyl carbinol. Seet-Amyl alcohol (1,1-Dimethylethyl) cyclohexane. Seet-Butylcyclohexane... [Pg.1424]

There exist three isomers of phenyl-propyl alcohol, all of which have been prepared and described, and, although not yet introduced into commerce, may eventually be so. These are as follows Benzyl-methyl-carbinol, CgHj. CHj. CH(OH)CHg, boiling at 215° phenyl-ethyl-carbinol, CgHg. CH(OH)CH2. CHg, boiling at 221° and benzyl-dimethyl-carbinol, C Hg. C(OH)(CHg)2, melting at 21° and boiling at 225°. [Pg.128]

To a solution of thienyl magnesium bromide prepared from 21.4 g of magnesium and 144 g of 2-bromothiophene are added 39.B g of ethyl 4-dimethylaminocyclohexylcarboxylate. The mixture is ailowed to warm to room temperature and stirred for an additional six hours. The reaction mixture is then decomposed with dilute ammonium chloride solution and extracted with ether. The combined ether extracts are extracted thoroughiy with 10% hydrochloric acid and the acid solution made alkaline with ammonium hydroxide. The aqueous solution is extracted with chloroform which is then washed with water, dried and evaporated to a residue in vacuo. Recrystallization of the residue from hexane yields Oi.O -dithienyl-4-dimethyl-aminocyclohexyl carbinol, melting point 156°C to 157°C after recrystallization from benzene. [Pg.1465]

Flowery Anisyl alcohol Benzyl acetate, phenylaceiate Cinnamic acid Cinnamyl acetate Citronellyl formate Crcsyl acetate Decanal Dimethyl benzyl carbinol Dimethyl benzyl carbinyl acetate Ethyl anthranilate Geranyl acetate Hydroxycitronellal dimethyl acetate Linalool Linalyl acetate Methyl benzoate Pcnethyl acetate 2-Phcnylpropionaldehyde 3-Phenylpropionaldehvde. [Pg.648]

Citronellal p-Citronellol Cyclohexyl acetate Cyclohexylethyl acetate Decanal Dihydro-3-ionone Dimethyl phenethyl carbinol Ethyl butyrate Ethyl caproate Ethylene brassylate... [Pg.5330]

Methylenebis(oxy) ]bis(2-chloroformaldehyde), see Bis (2-chloroethoxy) methane Methylene chlorobromide, see Bromochloromethane Methylene dichloride, see Methylene chloride Methylene dimethyl ether, see Methylal Methyl 2,2-divinyl ketone, see Mesityl oxide Methylene glycol, see Formaldehyde Methylene glycol dimethyl ether, see Methylal Methylene oxide, see Formaldehyde Methyl ethanoate, see Methyl acetate (1 -Methylethenyl)benzene, see a-Methylstyrene Methyl ethoxol, see Methyl cellosolve 1-Methylethylamine, see Isopropylamine (l-Methylethyl)benzene, see Isopropylbenzene Methylethyl carbinol, see sec-Bntyl alcohol Methyl ethylene oxide, see Propylene oxide ds-Methylethyl ethylene, see cis-2-Pentene frans-Methylethyl ethylene, see frans-2-Pentene Methyl ethyl ketone, see 2-Bntanone Methylethylmethane, see Butane... [Pg.1495]

The acetyl derivative (30) may be converted by Wolff-Kishner reduction into l,4-dimethyl-3-ethyl-3-piperideine (31).26 The latter compound is obtained in 17% yield also by dehydration of 1,4-dimethyl-3-( l-hydroxyethyl)piperidine (32) by the xanthate method.28 On the other hand, dehydration of the carbinol (32) with phosphorus pentoxide in toluene or by heating in concentrated hydrochloric aoid gives a mixture of isomeric l,4-dimethyl-3-ethylidenepiperidines (33a, b).28... [Pg.52]

Preparation of secondary (or tertiary) carbinols from pyridines and an aldehyde (or a ketone) in the presence of magnesium or aluminum and mercuric chloride is known in pyridine chemistry as the Emmert reaction. 7 70 For example, dimethyl-2-pyridylcarbinol is obtained in this way from pyridine and acetone. When a mixture of pyridine and acetone is subjected to an electrolytic reduction in dilute sulfuric acid at lead electrodes, a mixture of two main products results, namely, 2-(2-hydroxy-2-propyl)-3-piperideine and 4-(2-hydroxy-2-propyl)piperidine. Analogous compounds are obtained with the use of methyl ethyl ketone as the reactant. The mixed electrolytic reduction of 2-methylpyridine and acetone affords 2-(2-hydroxy-2-propyl)-6-methyl-3-piper ideine (74) and 2-methyl-4-(2-hydroxy-2-propyl)-piperidine.71... [Pg.67]

Reduction. The reagent is useful for reduction of carboxylic acid esters to primary alcohols. For example, the following esters have been reduced to the corresponding carbinols ethyl p-nitrobenzoate (96% yield), ethyl phenylacetate (90% yield), ethyl gly-cinate (70% yield). The reaction has some useful features Hydroxylic solvents (ethanol, water) can be used, the selectivity is higher than in the case of lithium aluminum hydride, and the reagent is nearly neutral. The reagent was found to be satisfactory for reduction of the dimethyl ester of 4,4 -dinitro-2,2 -diphenic acid (la) to the corresponding alcohol (lb, 51%yield).2... [Pg.305]

Ethyl-dimethyl-carbinol—Tertiary amylic alcohol—... [Pg.251]


See other pages where Dimethyl ethyl carbinol is mentioned: [Pg.276]    [Pg.1046]    [Pg.276]    [Pg.1046]    [Pg.1046]    [Pg.225]    [Pg.276]    [Pg.1046]    [Pg.61]    [Pg.1132]    [Pg.276]    [Pg.1046]    [Pg.432]    [Pg.276]    [Pg.1046]    [Pg.276]    [Pg.1046]    [Pg.1046]    [Pg.225]    [Pg.276]    [Pg.1046]    [Pg.61]    [Pg.1132]    [Pg.276]    [Pg.1046]    [Pg.432]    [Pg.444]    [Pg.97]    [Pg.370]    [Pg.149]    [Pg.153]    [Pg.289]    [Pg.296]    [Pg.648]    [Pg.289]    [Pg.296]    [Pg.54]    [Pg.71]    [Pg.743]    [Pg.132]   
See also in sourсe #XX -- [ Pg.260 ]

See also in sourсe #XX -- [ Pg.260 ]

See also in sourсe #XX -- [ Pg.260 ]

See also in sourсe #XX -- [ Pg.260 ]




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5.6- Dimethyl-2-[2- -ethyl

Carbinol

Carbinols

Dimethyl carbinol

Ethyl carbinol

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