《Steroid compounds. IX. Experiments on the synthesis of conessine. Synthesis of tetracyclic intermediates》 was published in Indian Journal of Chemistry in 1971. These research results belong to Mukharji, P. C.; Sircar, J. C.; Devasthale, V. V.. Application of 33797-34-1 The article mentions the following:
Condensation of 2-(2-methyl-3-methoxyphenyl)ethyl bromide with dimethyl cyclopentanone-2,3-dicarboxylate followed by cyclodehydration, catalytic hydrogenation and conversion of the secondary methoxycarbonyl group to a methyl ketone gave I. This, on Leuckart reaction with MeNHCHO gave stereospecifically II, which on reduction and demethylation gave the III, corresponding to the BCDE rings of conessine. Leuckart reaction of I and IV with HCONH2 gave a mixture of two epimeric lactams, in contrast to complete stereospecificity observed in the reaction with MeNHCHO. In addition to this study using (3-Methoxy-2-methylphenyl)methanol, there are many other studies that have used (3-Methoxy-2-methylphenyl)methanol(cas: 33797-34-1Application of 33797-34-1) was used in this study.
(3-Methoxy-2-methylphenyl)methanol(cas: 33797-34-1) belongs to ethers.The C-O bonds that comprise simple ethers are strong. They are unreactive toward all but the strongest bases. Although generally of low chemical reactivity, they are more reactive than alkanes. Application of 33797-34-1
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem