Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509180Generated: October 26, 2026

Triethylamine → 2-(4'-fluorobiphenyl-4-yl)-N-hydroxy-2-phenylacetamide

https://huagongshe.com/reaction/509180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant2-(4'-Fluorobiphenyl-4-yl)-2-phenylacetic acidHCID 57779683—
SolventPyridineHCID 1049—
Product2-(4'-fluorobiphenyl-4-yl)-N-hydroxy-2-phenylacetamideHCID 5777961348%

Reaction Steps

To a solution of 13 (40 mg, 0.14 mmol), BOP (58 mg, 0.13 mmol), and hydroxylamine hydrochloride (9 mg, 0.13 mmol) in pyridine (5 mL) was added triethylamine (0.055 mL, 0.39 mmol) and the reaction mixture was stirred at room temperature for 2 h. The solvents were removed under vacuum and the crude was dissolved in ethyl acetate. The organic layer was washed with water, dried over Na2SO4, filtered and concentrated. The residue was purified via HPLC (Gilson) reverse-phase column with a gradient of methanol (20-75%) in water to afford compound 14 as a white solid (20 mg, 48%). 1H NMR (CD3OD-d4) δ (ppm): 7.62-7.57 (m, 2H), 7.53 (d, J=8.2 Hz, 2H), 7.40-7.22 (m, 7H), 7.14 (t, J=8.8 Hz, 2H), 4.82 (s, 1H). LRMS (ESI): (calc.) 321.1 (found) 320.4 (MH)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096565B2
Source datasetuspto-grants-2015_08
ORD IDord-9f596383458f40dab57e980dd79d8e61
Source noteuspto-grants-2015_08