79744-78-8

Upstream product

• 3855-26-3 2-ethyl-4-methylphenol 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 
• 67609-56-7 1-ethyl-4-methyl-4-nitrocyclohexa-2,5-dienyl acetate 
• 1450-72-2 5-methyl-2-hydroxyacetophenone 
• 106-44-5 p-cresol 
• 105-67-9 2,4-Xylenol 
• 811-98-3 d⁽⁴⁾-methanol 
• 343942-17-6 1-ethyl-4-methyl-4-nitrocyclohexa-2,5-dienyl methyl ether 
• 64-67-5 diethyl sulfate 
• 104-93-8 p-methylanizole 

Downstream Products

• 91970-47-7 3-Aethyl-2-methoxy-5-methyl-benzoesaeure 
• 858854-30-5 1-(4-ethyl-5-hydroxy-2-methyl-phenyl)-ethanone 
• 3855-26-3 2-ethyl-4-methylphenol 
• 860734-42-5 2,5-diethyl-4-methyl-anisole 
• 93351-16-7 1-(4-ethyl-2-hydroxy-5-methyl-phenyl)-ethanone 
• 81591-15-3 3'-ethyl-5'-methyl-2'-hydroxy-acetophenone 

Relevant academic research and scientific papers

THIAZOLE COMPOUNDS USEFUL AS ACETYL-COA CARBOXYLASE (ACC) INHIBITORS

The present invention provides thiazole compounds of Formula I or its pharmaceutically acceptable salts, prodrugs, solvates, N-oxide thereof; solvates of pharmaceutically acceptable salts and N-oxides; pharmaceutically acceptable salts of N-oxides, or prodrugs; or combination or mixtures thereof; (I) The present invention further provides a method for preventing or treating a condition that responds to an Acetyl-CoA Carboxylase (ACC) inhibitor by using compounds of formula (I) or ), its pharmaceutically acceptable salts, prodrugs, solvates, N-oxide thereof; solvates of pharmaceutically acceptable salts and N-oxides; pharmaceutically acceptable salts of N-oxides, or prodrugs; or combination or mixtures thereof.

A New Rearrangement of Alkoxybenzyl Anions

Alkyl groups migrate from oxygen to carbon in alkyl aryl ethers which have been metalated in benzylic positions. 2,6-Dimethylanisole provides a variety of 2,6-dialkylphenols and their ethers in 45-80percent yields.Rearrangement products are obtained in 10-30percent yields from other dimethylanisoles and from methylanisoles.The reactions appear to proceed, like Wittig rearrangements, by homolytic cleavage of the alkyl-oxygen bond followed by recombination of the resulting radical pair in a different way.The rearrangements can be avoided by using methyl ethers and working at or below room temperature.

ipso Nitration. XXIII. Reactions of cyclohexadiene adducts from nitration of 4-ethyltoluene in acetic anhydride

The diastereoisomers of 4-ethyl-1-methyl-4-nitrocyclohexa-2,5-dienyl acetate (1) and 1-ethyl-4-methyl-4-nitrocyclohexa-2,5-dienyl acetate (2) are stereospecifically reduced to the corresponding nitrocyclohexadienols with aluminum hydride.Each dienol is stereospecifically methylated to the corresponding methyl ether with methyl iodide, silver oxide, and potassium hydroxide.Acid-catalysed solvolysis of the acetates 1 and 2 results in the substitution of the acetate moiety by other nucleophiles and these reactions are not stereospecific.The products of rearomatization of dienyl acetates, dienols and dienyl methyl ethers depend on the acidity and ionizing power of the solvents and are readily explained in terms of reactions involving a nitrocyclohexadienyl cation or acetoxy- (hydroxy-, methoxy-)cyclohexadienyl cation as key intermediates.In the 4-acetoxy-4-alkylcyclohexadienyl cation 1,2-migration of the acetoxyl group is more rapid then alkyl migration, but 1,2-alkyl migration is faster then migration of the hydroxyl or methoxyl groups in the corresponding cations. 1-Ethyl-4-methoxy-4-methylcyclohexa-2,5-dien-1-ol and 4-ethyl-3-nitrotoluene are significant minor products in the solvolysis of 1-ethyl-4-methyl-4-nitrocyclohexa-2,5-dien-1-ol in aqueous methanol.Nitration of p-ethyltoluene in the presence of sulfuric acid or in trifluoracetic anhydride gives a mixture of 4-ethyl-2-nitro- and 4-ethyl-3-nitrotoluene in a 2:1 ratio.