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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451099Generated: October 31, 2026

2,4-Dinitrophenol → HCID 10825027, compound

https://huagongshe.com/reaction/1451099

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DinitrophenolHCID 1493—
ReactantHCID 10593784HCID 10593784—
ReactantEthyl acetate hexaneHCID 21226206—
CatalystCopper oxideHCID 14829—
CatalystCupric ChlorideHCID 24014—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
ProductHCID 10825027HCID 1082502779%

Reaction Steps

A sample of 2-(methanesulfonylamino)-5-(methoxycarbonyl)benzaldehyde trimethylene mercaptal (7.66 g, 0.022 mol) dissolved in N,N-dimethylformamide (4.35 mL) and acetone (39.13 mL) was added over a 5-min period through a dropping funnel to a solution of copper (II) oxide (2.09 g, 0.026 mol), copper (II) chloride (7.0 g, 0.055 mol) in acetone (174.0 mL) and heated at reflux. After 2 h at reflux, thin-layer chromatography analysis (SiO2, EtOAc:hexane 1:1) showed disappearance of the starting material and the appearance of a new slightly higher Rf spot which gave a positive result when sprayed with 2,4-DNP. Upon cooling, the reaction was filtered through Celite and the cake was washed with 10% ethanol in dichloromethane. Water (125 mL) and dichloromethane (150 mL) were added to the filtrate. The layers were partitioned and the water layer extracted 2×100 mL dichloromethane. The combined organic layers were washed twice with water (100 mL), dried (Na2SO4), and filtered. Concentration of the filtrate gave a beige solid which was dried in vacuo to give 4.48 g (79%) of 2-(methanesulfonylamino)-5-(methoxycarbonyl)benzaldehyde, mp 161°-163° C. (ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602277
Source datasetuspto-grants-1997_02
ORD IDord-0953a01196a24ed9b92f0994ce3a095e
Source noteuspto-grants-1997_02