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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393571Generated: October 25, 2026

1-Naphthoic acid → 1-Naphthalenecarboxamide

https://huagongshe.com/reaction/393571

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Naphthoic acidHCID 6847—
ReactantN,N-DiethylanilineHCID 7061—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventTetrahydrofuranHCID 8028—
Product1-NaphthalenecarboxamideHCID 75244240.5%

Reaction Conditions

Temperature23 °C

Reaction Steps

Diethylaniline (0.27 μL, 1.7 μmol, 1.1 equiv) was added in one portion to a stirred solution of the amine (0.8 mg, 1.5 μmol, 1 equiv) in THF (0.2 mL) at 0° C. under an argon atmosphere and the solution was stirred for 5 min. 1-Naphthoic acid (0.34 mg, 2.0 μmol, 1.3 equiv), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.38 mg, 2.0 μmol, 1.3 equiv) and 1-hydroxybenzotriazole (0.25 mg, 1.8 μmol, 1.2 equiv) were then added separately, each in one portion, to the above solution at 0° C. The reaction mixture was warmed to 23° C. over 14 h 45 min, then was quenched with saturated aqueous ammonium chloride solution (3 mL). The mixture was diluted with ethyl acetate (10 mL) and the layers were separated. The aqueous layer was extracted with ethyl acetate (10 mL) and the combined organic layer was dried over sodium sulfate. Concentration in vacuo left a white solid, which was purified by flash column chromatography (80% ethyl acetate-hexanes) to give the naphthalene-1-carboxylic acid amide derivative (0.7 mg, 68%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809099B2
Source datasetuspto-grants-2004_10
ORD IDord-f64fe68ef4a84986b4c8e1dec4f0a7f2
Source noteuspto-grants-2004_10