ChemInform Abstract: ACID-CATALYZED REACTIONS OF AROMATICS WITH ALKANES AND CYCLOALKANES. VIII. PROMOTER EFFECT OF ISOBUTANE DURING THE UNCONVENTIONAL FRIEDEL-CRAFTS ALKYLATION OF BENZENE AND TOLUENE WITH CYCLOHEXANE

1978 ◽  
Vol 9 (8) ◽  
Author(s):  
R. MIETHCHEN ◽  
A. GAERTNER ◽  
C.-F. KROEGER
1966 ◽  
Vol 44 (15) ◽  
pp. 1809-1816 ◽  
Author(s):  
J. M. Pepper ◽  
B. P. Robinson

In part II of this series the isolation and identification of nine products from the reaction of vinyl acetate with benzene and aluminium chloride were described. This paper presents a discussion of the mechanism of formation of these compounds.A comparison of the aluminium chloride catalyzed reactions of benzene with vinyl acetate and ethyl acetate is described. The reaction with ethyl acetate gave all the monocyclic products obtained from the reaction involving vinyl acetate, as well as m-diethylbenzene. The ratio of the ortho and para isomers of ethylacetophenone is the same in both reactions, which suggests that the same acetylating species is involved. The fact that none of the three polycyclic products is obtained from the reaction involving ethyl acetate suggests that the vinyl moiety of the ester is involved in the formation of these compounds from vinyl acetate. The use of 14C-labelled vinyl acetate confirmed the fact that the synthesis of 9,10-dimethylanthracene involved only the vinyl part of the ester.A study of the reactions of ethyl acetate and vinyl acetate with aluminium chloride showed that ethyl chloride and vinyl chloride, respectively, may be intermediates in the alkylation of benzene with these reagents. Evidence is presented that 1-phenylethyl chloride may also be an intermediate product in the reaction of vinyl acetate and benzene. 1,1-Diphenylethane is believed to be involved in the formation of 9,10-dimethylanthracene, the final step of which is thought to occur by the dehydrogenation of 9,10-dihydro-9,10-dimethylanthracene.


1986 ◽  
Vol 51 (10) ◽  
pp. 2167-2180 ◽  
Author(s):  
Lubor Fišera ◽  
Nadezhda D. Kozhina ◽  
Peter Oravec ◽  
Hans-Joachim Timpe ◽  
Ladislav Štibrányi ◽  
...  

3-Aryl-4-R-carbamoyl-5-hydroxymethylisoxazolines (IV) were synthesized by allowing R-NH2 amines with R = H, CH3, C3H7, C6H5C2H5, and NH2 to act on 3-(X-phenyl)-4-oxo-3a,4,6,6a-tetrahydrofuro[3,4-d]isoxazoles (III) with X = H, 4-CH3, 4-OCH3, 2-OCH3, 4-Cl, 2-Cl, 4-F, 2-F, 4-Br, 4-NO2, and 3-NO2. Exposed to radiation, the substances IV give Z-2-hydroxymethylamino-2-aryl-1-formylacrylamides (V) in good yields. The 4-Cl and 4-F substituted Z-derivatives V isomerize irreversibly to the E-derivatives VI if allowed to stand in solvent; the remaining derivatives V are stable. The quantum yields of the photoreaction are from 0.012 to 0.106 in dependence on the substituent X. In all cases where the compounds IV were used for the preparation of condensed heterocycles in conditions of acid-catalyzed reactions, lactones III were preferentially formed; the action of thionyl chloride on IV results in the formation of chloromethyl derivatives VIII, which do not undergo further cyclization.


Author(s):  
Mizzanoor Rahaman ◽  
M. Shahnawaz Ali ◽  
Khorshada Jahan ◽  
Damon Hinz ◽  
Jawad Bin Belayet ◽  
...  

Author(s):  
Emanuele Moioli ◽  
Leo Schmid ◽  
Peter Wasserscheid ◽  
Hannsjoerg Freund

The kinetics of the acid catalyzed reactions of acetaldehyde ammonia trimer (AAT) and paraldehyde (para) to 2-methyl-5-ethyl pyridine (MEP) in the presence of an acid catalyst were investigated systematically. A...


ChemInform ◽  
1987 ◽  
Vol 18 (47) ◽  
Author(s):  
S. V. CHAPYSHEV ◽  
L. I. KIRKOVSKII ◽  
V. G. KARTSEV

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