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2.4- Dinitro-benzenesulfonyl chloride

Transformation of a primary amine to a secondary amine using 2,4-dinitro-benzenesulfonyl chloride and an alcohol. Also known as Fukuyama-Mitsunobu procedure. [Pg.247]

The hydrazine can be prepared in 70% yield by the reaction of 2,4-dinitro-benzenesulfonyl chloride with 95% hydrazine in THF at -78 65°. [Pg.232]

Benzene, (cHLORO-teri-BuTYL)-, 32, 90 2-chloro-1, 3-dinitro-, 32, 23 ETHYNYL-, 30, 72 HEXAMETHYL-, 35, 73 1,2,3-trimethyl-, 34, 56 Benzeneboronic ACID, 39, 4 Benzeneboronic anhydride 39, 3 Benzenediazonium chloride, 32, 84 Benzenesulfenyl chloride, 36, 101 Benzenesulfonyl chloride, 31, 83 9,10-o-Benzenoanthracene, 9,10-dihydro-, 39, 75 Benzhydrol, 33, 11 Benzhydryl chloride, 39, 74 Benzidine, 36, 21... [Pg.85]

See other pages where 2.4- Dinitro-benzenesulfonyl chloride is mentioned: [Pg.359]    [Pg.45]    [Pg.94]   
See also in sourсe #XX -- [ Pg.243 ]

See also in sourсe #XX -- [ Pg.153 ]

See also in sourсe #XX -- [ Pg.243 ]



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