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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058653Generated: October 31, 2026

Sodium Hydroxide → 2-[(2-Chlorophenyl)sulfanyl]-5-nitrobenzaldehyde

https://huagongshe.com/reaction/1058653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactanto-ChlorothiophenolHCID 80599—
Reactant2-Fluoro-5-nitrobenzaldehydeHCID 2734770—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product2-[(2-Chlorophenyl)sulfanyl]-5-nitrobenzaldehydeHCID 1866899985.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

A 2.5 mol/L sodium hydroxide aqueous solution (1.7 mL, 4.4 mmol) and tetrabutylammonium bromide (0.017 g, 0.051 mmol) were added to 2-chlorobenzenethiol (0.17 g, 1.0 mmol), followed by stirring at 25° C. for 10 minutes. To the reaction liquid was added a toluene (1.7 mL) solution of 2-fluoro-5-nitrobenzaldehyde (0.18 g, 1.0 mmol), followed by stirring at 110° C. for 2 hours. After the conventional post-reaction treatment, the residue was purified by silica gel chromatography (eluted by chloroform) to give 2-[(2-chlorophenyl)thio]-5-nitrobenzaldehyde (0.25 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518268B1
Source datasetuspto-grants-2003_02
ORD IDord-b1d3b367fdf04450b920786fa93d2ed6
Source noteuspto-grants-2003_02