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George Mason University

Fuctionalized Alkyl Quinolines: Synthesis and Characterization

Abstract

Novel syntheses using 4-methoxy-2-methylquinoline were attempted by using a strong base to remove the most acidic proton, one of the protons of the methyl in the 2-position, to generate a carbanion. Upon the introduction of a halide with an electrophile, the electrophile will attack the carbanion where the proton was removed in an SN2 reaction to make a new compound. The methods for how this type of reaction was tried were attempted temperatures and bases are described. The DEPT-90 and 135 of 4-methoxy-2-methylquinoline were run, analyzed and the spectra are given. The DEPT spectra for this compound constitute a new contribution to the reference information for 4-methoxy-2-methylquinoline.

Author and committee

dc:creator, dc:contributor.*
Author
  • Dripps, Rachel B.

Subjects

dc:subject × 4

Identifiers

dc:identifier.*
Identifier
hdl:1920/5613
OAI identifier oai:identifier
oai:MARS:1920/5613

Chain of custody

source
Harvested from
George Mason University
Base URL
mars.gmu.edu/server/oai/request
Last updated
2026-07-27
Source record
OAI-PMH GetRecord
citation

Dripps, Rachel B.. Fuctionalized Alkyl Quinolines: Synthesis and Characterization. 2009.