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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167175Generated: November 1, 2026

Hydrochloric Acid → 2-Amino-3-methoxybenzaldehyde

https://huagongshe.com/reaction/1167175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Methoxy-2-nitrobenzaldehydeHCID 98867—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Amino-3-methoxybenzaldehydeHCID 13970121112.6%

Reaction Steps

5 g of 3-methoxy-2-nitrobenzaldehyde are dissolved in a solution of 100 ml of ethanol, 100 ml of acetic acid and 50 ml of water. After addition of 11.4 g of iron and of 1.4 ml of concentrated hydrochloric acid, the reaction medium is heated at reflux for 10-15 minutes. After having cooled the reaction medium, 150 ml of water are added and the reaction mixture is extracted with 3×200 ml of dichloromethane. The organic phases are combined, washed with 500 ml of a saturated sodium hydrogencarbonate solution, dried over magnesium sulfate, filtered and evaporated under vacuum to provide 4.7 g of 3-methoxy-2-aminobenzaldehyde in the form of a colorless oil, used without purification in the following stage. (Yield: quantitative)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617336B1
Source datasetuspto-grants-2003_09
ORD IDord-bdc97d47f63e4ce1bfc15a2bf8443b97
Source noteuspto-grants-2003_09