STUDY AND SYNTHESIS OF DIATYCLIC REACTIONS OF 1-TIAIN, 1-THIOCHROMAN AND THEIR PRODUCTS
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Abstract
The paper examines the diacylation reaction of 1-thiaine, 1-thiochroman, 2,5-dimethyl-1-thiaine and 6-methyl-1-thiochroman with acetic acid chlorohydride in dichloromethane solution in the presence of the AlCl3 catalyst. As a result of the reaction, it was found that 1-thiaindane, 1-thiochroman and 2-methyl-1-thiainides do not undergo diacylation reactions in the presence of large amounts of catalysts and acylating agents. However, 2,5-dimethyl-1-thian and 6-methyl-1-thiochromans undergo acetic acid chlorohydride to form a large number of acylating agents and catalysts in the diacylation reaction, resulting in the formation of 2,5-dimethyl-3,6-diacetyl-1-thiaine. detected.
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References
Wang X, Wang Y, Da-Ming Du and Xu J. Solvent-free, AlCl3-promoted tandem Friedel–Crafts reaction of arenes and aldehydes. J of Molecular Catalysis A: Chemical. 2006;255:31–35
Monat Hosseini Sarvari, Hashem Sharghi. Simple and Improved Procedure for the Regioselective Acylation of Aromatic Ethers with Carboxylic Acids on the Surface of Graphite in the Presence of Methanesulfonic Acid SYNTHESIS 2004, No. 13, pp 2165–2168x.x.204
E.G.Derouane, G.Crehan, C.J.Dillon, D.Bethell, H.He, S.B.Abd Hamid, J.Catal. 194 (2000) 410.
B.M.Devassy, S.B.Halligudi, C.G.Hedge, A.B.Halgeri, F.Lefebvre, Chem. Commun. (2002) 1074.
J. Kaur, K. Griffin, B. Harrison, I.V. Kozhevnikov, J. Catal. 208 (2002) 448.