The reactions of substituted naphthalenes with butyl mercaptides
Abstract
The reactions of butyl mercaptides with fluoro-, bromo-, nitro-, and methoxynaphthalenes in DMSO and methanol have been studied. The halonaphthalene reactions gave reasonably good yields of alkyl naphthyl sulfides via direct nucleophilic substitution. 1-Halonaphthalene gave only 1-substituted alkyl naphthyl sulfide and 2-halo- naphthalenes gave only 2-substituted alkyl naphthyl sulfides. No alkyl naphthyl sulfide was produced from either methoxynaphthalene or nitronaphthalene.
Degree
MS
College and Department
Physical and Mathematical Sciences; Chemistry and Biochemistry
Rights
http://lib.byu.edu/about/copyright/
BYU ScholarsArchive Citation
South, John Allan, "The reactions of substituted naphthalenes with butyl mercaptides" (1972). Theses and Dissertations. 8358.
https://scholarsarchive.byu.edu/etd/8358
Date Submitted
1972-08-01
Document Type
Thesis
Handle
http://hdl.lib.byu.edu/1877/Letd665
Keywords
Naphthalene, Thiols
Language
English