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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421999Generated: October 26, 2026

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

https://huagongshe.com/reaction/2421999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyBOPHCID 2724699—
Reactant2-[4-(Trifluoromethoxy)phenyl]acetic acidHCID 2777319—
SolventDimethylformamideHCID 6228—
Product2-[4-(Trifluoromethoxy)phenyl]acetamideHCID 1870359357.3%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960380B2
Source datasetuspto-grants-2011_06
ORD IDord-ecb58508def0432e9d3d92e0868a3c1a
Source noteuspto-grants-2011_06