PyBOP → 2-[4-(Trifluoromethoxy)phenyl]acetamide

4-(Trifluoromethoxy)phenylacetic acid (2 g, 9.085 mmol) was dissolved in DMF (20 ml, dry) and PyBOP (4.728 g, 9.085 mmol) was added. The mixture was stirred in an ice-bath and ammonia gas was bubbled in for 5 mins. The ice-bath was removed and the mixture was stirred at rt overnight and then evaporated in vacuum. Water (50 ml) was added into the residue and it was extracted with EtOAc (20 ml×3). The extracts were combined, washed with saturated aqueous NaHCO3 (15 ml), water (20 ml×3), brine (15 ml), dried (MgSO4) and evaporated. The residue was purified by column chromatography (ISOLUTE SI, 20 g/70 ml), eluting with DCM, then MeOH/DCM (1:99), to give the title compound (1.14 g, 57%) as a white solid. Mass Spectrum: M−H+ 218. 1H NMR (400 MHz, CD3OD): δ 3.53 (s, 2H), 7.20 (d, 2H), 7.38 (d, 2H). 13C NMR (100 MHz, CD3OD): 42.5, 121.9 (q, J=253 Hz), 122.1, 131.8, 136.3, 149.4, 176.2.

1. customammonia gas was bubbled in for 5 mins
2. customThe ice-bath was removed
3. stirringthe mixture was stirred at rt overnight
4. customevaporated in vacuum
5. additionWater (50 ml) was added into the residue and it
6. extractionwas extracted with EtOAc (20 ml×3)
7. washwashed with saturated aqueous NaHCO3 (15 ml), water (20 ml×3), brine (15 ml)
8. dry with materialdried (MgSO4)
9. customevaporated
10. customThe residue was purified by column chromatography (ISOLUTE SI, 20 g/70 ml)
11. washeluting with DCM

ORD record

ord-69cb31470bc44521800d036076aa95be

Source dataset

uspto-grants-2010_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07723333B2