“…A mixture of compound A (3.00 g, 10.44 mmol) and 1-bromotetradecane (8.72 g, 31.49 mmol) in acetone (30 mL) was refluxed for 24 h. After the reaction mixture had cooled to room temperature, the crude product was isolated by filtering and then recrystallized twice from a mixture of acetone and acetonitrile to give 14-DEHA-14 as white crystal (8.04 g, yield 91.60 %). 1 H NMR (400 MHz, CDCl 3 ) d ppm: 0.86-0.89 (t, J = 6.8 Hz, 6H, 2(CH 2 ) 11 CH 3 ), 1.25-1.36 (m, 44H, 2(CH 2 ) 11 CH 3 ), 1.70-1.77 (m, 8H, CH 2 CH 2 CH 2 CH 2 and 2CH 2 CH 2 (CH 2 ) 11 ), 2.44 (m, 4H, 2CH 2 COO), 3.48 (s, 12H, 4NCH 3 ), 3.62-3.66 (t, J = 7.6 Hz, 4H, 2 NCH 2 CH 2 (-CH 2 ) 11 )…”