Edge Rewrite
// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a248e16a0f268020

Jump to content

Sulfamation

From Wikipedia, the free encyclopedia

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

[edit]
  1. DuBois, Grant E.; Stephenson, Rebecca A. (1980). "Sulfonylamine-Mediated Sulfamation of Amines. A Mild, High Yield Synthesis of Sulfamic Acid Salts". The Journal of Organic Chemistry. 45 (26): 5371–5373. doi:10.1021/jo01314a033.