n1-Isopropoxy-3-nitro-1-benzenesulfonamide → 3-Amino-n1-isopropoxy-1-benzenesulfonamide

Participants

Reaction Steps

To a Parr H2 vessel containing 5% Pd/BaSO4 (0.350 g) was added a methanolic solution (125 mL) of N1-isopropoxy-3-nitro-1-benzenesulfonamide (3.50 g, 0.0135 mol) at rt under Ar atm. The solution was hydrogenated at 45 psi for approx. 1.0 h. The reaction mixtire was filtered (½″ celite pad) and evaporated to give the product as yellow crystalline solid 2.90 g (96%). 1H NMR (CDCl3) 1.20(d,25H); 4.27(m, 1H); 7.05(s,1H); 7.75(1,1H); 8.22(d, 1H); 8.48 (dd,1H); 8.74(t, 1H).

Provenance & Evidence