The system aluminum chloride-acetyl chloride in sulfur dioxide solvent

1982 ◽  
Vol 47 (6) ◽  
pp. 1005-1007 ◽  
Author(s):  
Boris Glavincevski ◽  
Sydney Brownstein
1999 ◽  
Vol 64 (1) ◽  
pp. 99-106
Author(s):  
Battsengel Gotov ◽  
Štefan Toma ◽  
Eva Solčániová

Acetylations of 3-ferrocenyl-1-methylpyrrole as well as 3-cyano-4-ferrocenylpyrrole and 3-cyano-4-ferrocenyl-1-methylpyrrole were performed. The course of the acylation is highly dependent on the acylation agent, that is acetyl chloride/aluminum chloride (method A), trifluoroacetic anhydride-acetic acid mixture (method B) or acetic anhydride/Sc(OTf)3 (method C). Method A gives the acetylation on ferrocene moiety, method B affords the trifluoroacetylation on pyrrole moiety and method C affords pyrrole moiety acetylation. Vielsmeier-Haack formylation gives the products of substitution on pyrrole moiety.


1964 ◽  
Vol 42 (4) ◽  
pp. 717-723 ◽  
Author(s):  
R. C. Mehrotra ◽  
R. A. Misra

The reactions between aluminum tertiary butoxide and acetyl chloride have been studied. The addition of 1 mole of acetyl chloride to aluminum tertiary butoxide forms monochloride ditertiary butoxide, which, with another mole of acetyl chloride, appears to give the dichloride monotertiary butoxide derivatives. Further, these products appear to react with tertiary butyl acetate formed in the reaction itself, giving acetate derivatives. The above is confirmed by a detailed study of the reactions between aluminum chloride and tertiary butyl acetate, which have been found to result in the acetate derivatives. A plausible mechanism has been suggested.


1982 ◽  
Vol 47 (24) ◽  
pp. 4737-4739 ◽  
Author(s):  
Liang K. Tan ◽  
Sydney Brownstein

1969 ◽  
Vol 10 (30) ◽  
pp. 2581-2584 ◽  
Author(s):  
I. Tabushi ◽  
K. Fujita ◽  
R. Oda ◽  
M. Tsuboi

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