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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990256Generated: October 30, 2026

Hexafluorophosphate → HCID 18420299, compound

https://huagongshe.com/reaction/990256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexafluorophosphateHCID 9886—
Reactant4-Acetylbenzoic AcidHCID 11470—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 18369529HCID 18369529—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 18420299HCID 1842029999%

Reaction Steps

N-{2-Oxo-2-{di(phenylmethyl)amino}ethyl}-4-acetylbenzamide: To a solution of 4-acetylbenzoic acid (1.21 g, 7.37 mmol) in DMF (35 mL) was added successively the product of the preceding section (b) (2.03 g, 7.0 mmol), DIPEA (4.3 mL, 24.5 mmol) and BOP.PF6 (3.25 g, 7.37 mmol). The resulting solution was stirred at room temperature for 2 h, then diluted with EtOAc, washed serially with H2O, 4N aqueous HCl, saturated NaHCO3, and brine, dried (MgSO4) and concentrated under reduced pressure to give N {2-oxo-2-{di(phenylmethyl)amino}ethyl}-4-acetylbenzamide (2.70 g, 99% yield) as a light yellow foam: 1H NMR (400 MHz, DMSO-d6) 8 8.89 (t, 1H, J=5.7 Hz), 8.05 (d, 2H, J=8.4 Hz), 8.00 (d, 2H, J=8.4 Hz), 7.24-7.44 (m, 10 H), 4.61 (s, 2H), 4.51 (s, 2H), 4.25(d, 2H, J=5.7 Hz), 2.52 (s, 3H); MS (FAB) m/z 401 (MH)+. This product was used as such in the next reaction (section (d)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458959B1
Source datasetuspto-grants-2002_10
ORD IDord-f0c8ac306c7a4094b4abb611f6139707
Source noteuspto-grants-2002_10