In organic chemistry sulfamation is the installation of either of two related functional groups, sulfamic acid (R2NSO3H) and sulfamate (R2NSO3−). Typical methods entail reaction of primary amines with sources of sulfur trioxide such as pyridine-sulfur trioxide:[1]
- RNH2 + SO3 → RNHSO3H
Sulfamation can also be effected by treating the amine with the sulfate ester of catechol (C6H4O2SO2).
References
- ^ DuBois, Grant E.; Stephenson, Rebecca A. (1980). 「スルホニルアミンを介したアミンのスルファム化.スルファミン酸塩の温和で高収率な合成」. The Journal of Organic Chemistry . 45 (26): 5371– 5373. doi :10.1021/jo01314a033.