“…After the completion of the reaction and the workup process, the solvent was removed under reduced pressure to form a residue, which was chromatographed on a silica gel column with n -hexane/dichloromethane (V/V 3:1) as an eluent to yield a yellow powder as a TPA-CHO product. (346 mg, 96.0% yield). − 1 H NMR (400 MHz, CDCl 3 ) δ/ppm: 10.02 (s, 1H −CHO), 7.91–7.93, (dd, J = 6.4, 6.8 Hz, 2H −Ar–H), 7.71–7.73, (d, J = 8 Hz, 2H, −Ar–H), 7.506–7.528 (dd, J = 8.8 Hz, 2H, −Ar–H), 7.255–7.308 (q, J = 7.2, 6.4 Hz, 4H −Ar–H), 7.130–7.158 (m, J = 8 Hz, 6H, −Ar–H), 7.048–7.090 (t, J = 7.2, 7.6 Hz, 2H −Ar–H). 13 C NMR: (101 MHz, CDCl 3 ) d/ppm: 192.08, 148.66, 147.57, 146.86, 134.92, 133.02, 130.57, 129.64, 128.26, 127.13, 123.71, 123.35.…”