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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253313Generated: October 28, 2026

Chloranil → HCID 178472256, compound

https://huagongshe.com/reaction/2253313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloranilHCID 8371—
Reactant2-MethoxybenzaldehydeHCID 8658—
ReactantHCID 59645484HCID 59645484—
SolventAcetonitrileHCID 6342—
ProductHCID 178472256HCID 17847225671%

Reaction Steps

A solution of diethyl [3,4-diamino-2-(methoxycarbonyl)phenyl]malonate (4.39 g, 13.5 mmol), 2-methoxybenzaldehyde (1.97 g, 14.5 mmol) and p-chloranil (6.10 g, 14.5 mmol) in MeCN (135 mL) was stirred at room temperature for 22 h. The resulting suspension was filtered and the solid recovered was washed with MeCN (filtrate 1 kept). The solid was dissolved in EtOAc (800 mL) and the resulting solution was successively washed with aqueous 1N NaOH solution (3×150 mL), water (150 mL) and brine (100 mL), dried (MgSO4), filtered and concentrated under reduced pressure. The resulting solid was triturated with hexane:EtOAc (1:1; 135 mL) to give the title compound (4.22 g) as a white solid (filtrate 2 kept). The filtrates 1 and 2 were combined and concentrated under reduced pressure. The residue was treated as the initial solid but the residue after washings was concentrated and purified by flash chromatography (10-40μ silica gel; hexane:EtOAc 1:1) before being triturated with hexane:EtOAc (3:2; 35 mL) to give an additional 0.72 g amount (total of 4.96 g, 83% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323567B2
Source datasetuspto-grants-2008_01
ORD IDord-8bc6520a868846ea9501334b697e2239
Source noteuspto-grants-2008_01