1950
DOI: 10.1021/jo01148a028
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Sulfones. Ii. Derivatives of 4,4'-Diaminodiphenyl Sulfone

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Cited by 9 publications
(4 citation statements)
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“…The mixture was heated to boiling, cooled and filtered; yield, 86%, m.p., 228°dec. This compound did not hydrolyze to X, but was recovered unchanged, when heated at 50°in 96% sulfuric acid, a hydrolysis reaction usually useful for N-arylsulfonamides (5). Hydrochloric acid hydrolysis removed the methylmercapto group as expected (7).…”
Section: -167°mentioning
confidence: 77%
“…The mixture was heated to boiling, cooled and filtered; yield, 86%, m.p., 228°dec. This compound did not hydrolyze to X, but was recovered unchanged, when heated at 50°in 96% sulfuric acid, a hydrolysis reaction usually useful for N-arylsulfonamides (5). Hydrochloric acid hydrolysis removed the methylmercapto group as expected (7).…”
Section: -167°mentioning
confidence: 77%
“…Subsequently, the nitro group is reduced to the free amino function using hydrogen and Raney nickel. In a final reaction step, the protecting group has to be removed and gives 4‐[(4‐aminophenyl)sulfonyl]‐ N ‐propylaniline in an overall yield of 79% 16. The synthesis protocol developed by us allows us to isolate product 5b in a yield of 86% in only one step.…”
Section: Resultsmentioning
confidence: 99%
“…N-p-Tosylamino-p'-nitrophenyl sulfide. After this paper was prepared for publication an account of the preparation of this compound by Baker, Querry, and Kadish appeared (21). They reported m.p.…”
Section: Discussion and Proceduresmentioning
confidence: 99%