3-Chloro-4-isopropoxybenzaldehyde → 3-Chloro-4-(propan-2-yloxy)benzoic acid

Participants

Reaction Steps

When the 3-chloro-4-isopropoxybenzaldehyde was substituted for 3-chloro-4-ethoxybenzaldehyde in Example 49, Step A the identical process afforded the title compound in 98% yield, as a colourless solid. 1H-NMR (CDCl3) 1.4 (d, 6H, J=5.1 Hz); 4.67 (m, 1H); 6.95 (m, 1H); 7.96 (m, 1H); 8.10 (m, 1H).

Provenance & Evidence