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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374065Generated: October 30, 2026

N-Hydroxyphthalimide → HCID 21075918, compound

https://huagongshe.com/reaction/1374065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantNaproxenHCID 156391—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 21075918HCID 2107591847%

Reaction Steps

A mixture of N-hydroxyphthalimide (7.1 g, 43.4 mmol), (2S)-2-(6-methoxy(2-naphthyl))propanoic acid (naproxen, 10 g, 43.4 mmol) and N,N-dimethylaminopyridine (DMAP, 5.3 g, 43.4 mmol) in CH2Cl2 (70 mL) and DMF (30 mL) at 0° C. was treated with 1-(3-(dimethylamino)propyl)-3-ethylcarbodiimide hydrochloride (8.3 g, 43.4 mmol) in CH2Cl2 (50 mL). The reaction mixture was stirred at room temperature for 16 hours and the solvent was evaporated under vacuum. The residue was then dissolved in EtOAc, washed with brine, dried over Na2SO4 and filtered. The residue after evaporation of the solvent was chromatographed on silica gel eluting with EtOAc hexane (1:1) to give the title compound (7.6 g, 47% yield) as a white solid. Mp 110–112° C. 1H NMR (300 MHz, d6-DMSO) δ 7.80–8.06 (m, 7H), 7.50 (dd, J=1.7 and 8.5 Hz, 1H), 7.32–7.37 (m, 1H), 7.20 (dd, J=2.5 and 9.0 Hz, 1H), 4.50 (q, J=7.1 Hz, 1H), 3.89 (s, 3H), 1.64 (d, J=7.1 Hz, 3H). 13C NMR (75 MHz, d6-DMSO) δ 171.2, 161.8, 157.5, 153.0, 135.5, 133.6, 133.5, 129.3, 128.4, 128.2, 127.3, 126.1, 126.0, 124.0, 119.0, 105.8, 55.2, 41.8, 18.6. Mass spectrum (API-TIS) m/z 376 (MH+), 393 (MNH4+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163958B2
Source datasetuspto-grants-2007_01
ORD IDord-ab18a3e75252422caf221c733ca46753
Source noteuspto-grants-2007_01