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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213835Generated: October 30, 2026

Nitric Acid → 4-(2-Chloroethoxy)-5-methoxy-2-nitrobenzaldehyde

https://huagongshe.com/reaction/2213835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
Reactant4-(2-Chloroethoxy)-3-methoxybenzaldehydeHCID 10775023—
Solvent1,2-DichloroethaneHCID 11—
Product4-(2-Chloroethoxy)-5-methoxy-2-nitrobenzaldehydeHCID 2195638240%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Fuming nitric acid (10 mL) is added dropwise to a −40° C. suspension of 5.00 g (23.36 mmol) of 4-(2-chloroethoxy)-3-methoxybenzaldehyde (Milbank, J. B. J., et. al., J. Med. Chem., 42(4), 649–658, 1999) in 23 mL of 1,2-dichloroethane. The reaction mixture is slowly allowed to warm to −10° C. The mixture is poured onto 300 mL of ice water and then extracted with ethyl acetate. The organic layer is dried over magnesium sulfate, filtered and concentrated in vacuo. Diethyl ether is added to the residue and the pale yellow solid is collected by filtration to provide 2.43 g (40%) of 4-(2-chloroethoxy)-5-methoxy-2-nitrobenzaldehyde, mp 148–150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105531B2
Source datasetuspto-grants-2006_09
ORD IDord-328218e672dc469c9550b35cee734642
Source noteuspto-grants-2006_09