Navigation

0 Hits

  • Previous / Next

You are using Science Of Synthesis as a Guest.
Please login to access the full content or check if you have access via
40.11.5.1.1 Method 1: Synthesis via Reaction of Anilines with Disulfur Dichloride

DOI: 10.1055/sos-SD-040-00963

Chemler, S. R.Science of Synthesis, (2009401278.

2,4-Di-tert-butyl-6-methyl-N-thiosulfinylaniline (27) has been synthesized in very good yield by condensation of 2,4-di-tert-butyl-6-methylaniline (26) with sulfur monochloride (Scheme 14).[‌55‌] However, the reaction is not general, and other anilines either do not provide the N-thiosulfinylarylamines or provide them in low yields along with other compounds.

Meeeee 88 Meeeeeeee ee 8,8-Me-eeee-eeeee-8-eeeeee-M-eeeeeeeeeeeeeeeeeee[‌88‌]

Meeeeeeeeeee Meeeeeeee

8,8-Me-eeee-eeeee-8-eeeeee-M-eeeeeeeeeeeeeeeeeee (88):[‌88‌]

MMMMMMM: Meeeee eeeeeeeeeeee ee ee eee, eeee, eee eeeeee eeeeeeee eeeeeeee. Me ee eeee e eeeeeeeeeee eee eeeeee eeeeeeeee eeee eeeee.

M eeee ee M8Me8 (888ee, 8.88eeee) ee Me8M (8.8eM) eee eeeee eeeeeeee ee e eeee ee 8,8-ee-eeee-eeeee-8-eeeeeeeeeeeee (88; 888ee, 8.88eeee) eee Me8M (888ee, 8.8eeee) ee Me8M (88eM) eeee eeeeeeee ee 8°M. Meeee eeeee eeeeeee eee 8e, eee eeeeeee eee eeeeee eeee M8M, eee eee eeeeeee eeeee eee eeeee (MeMM8). Meeeeee ee eee eeeeeee eeee e eeee eeeeee eee, eeeee eee eeeeeeeee ee eeeeeeeeeeeeeee eeeeeeeeee (eeeeee eee, eeeeee). Mee eeeee eeeeeeee eeee 88ee ee eeeeee. Mee eeeeee eeeeee eeeeeeee eeee eee eeeeeee ee e eeee eeeeee eee, eeeee eeeeeeeeeeee eeee eeeeeeee. Meeeeeee eeeeeeeeeeeeeeeeee (ee MeMM) eeeeeeee ee eeeeeeeeeeee eeee eeeeeeee ee 88; eeeee: 8.88e (88%); ee 8888°M.

References


Cookie-Einstellungen