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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244420Generated: October 26, 2026

1-Naphthoic acid → 1-Naphthalenecarboxamide

https://huagongshe.com/reaction/1244420

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 numberUS07122549B2
Source datasetuspto-grants-2006_10
ORD IDord-09cf1e32645940d68ece7fa7c07a2a6a
Source noteuspto-grants-2006_10