C(OC([NH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[F:15])=O)(C)(C)C.[CH3:16][S:17]SC>>[F:15][C:10]1[CH:11]=[CH:12][CH:13]=[C:14]([S:17][CH3:16])[C:9]=1[NH2:8]This material was prepared for N-t-butoxycarbonyl-2-fluoroaniline and dimethyl disulfide following the general procedure outlined in Example 102. IR and 1H NMR spectra of the product were consistent with the assigned structure.
Wird geladen…