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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581953Generated: November 4, 2026

2-Naphthalenecarboxaldehyde → N-[6{(Naphthalen-2-ylmethyl)-amino}-hexyl]-2-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1581953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphthalenecarboxaldehydeHCID 6201—
ReactantN-(6-Aminohexyl)-2-nitrobenzenesulfonamide HydrochlorideHCID 22719658—
SolventTolueneHCID 1140—
ProductN-[6{(Naphthalen-2-ylmethyl)-amino}-hexyl]-2-nitrobenzenesulfonamideHCID 1204230137%

Reaction Steps

A mixture of N-(6-Aminohexyl)-2-nitrobenzenesulfonamide hydrochloride (0.67 g, 2.0 mmol) and 2-naphthaldehyde (0.32 g, 2.1 mmol) in 75 mL of toluene was refluxed using a Dean Stark trap for 20 h. The reaction mixture was concentrated in vacuo. The residue was dissolved in ethanol (40 mL) and sodium borohyride (0.020 g,6.0 mmol) was added. After the reaction was complete (6 h), the solvent was evaporated and residue taken up in 30 mL of saturated sodium chloride solution and extracted with ethyl acetate(3×40mL), washed with saturated sodium chloride solution, dried over sodium sulfate and concetrated to afford an oil. The oil was flash chromatographed over silica gel to afford the titled compound (0.16 g, 37%) which was converted into hydrochloride salt (mp 169° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734182B2
Source datasetuspto-grants-2004_05
ORD IDord-4e6ec25be37140a6ba48e3421121f769
Source noteuspto-grants-2004_05