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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075434Generated: October 30, 2026

Hydrochloric Acid → 4-Dimethoxymethyl-1-(2-morpholinoethoxy)-2-nitrobenzene

https://huagongshe.com/reaction/2075434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl orthoformateHCID 9005—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Morpholinoethoxy)-3-nitrobenzaldehyde hydrochlorideHCID 23117920—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product4-Dimethoxymethyl-1-(2-morpholinoethoxy)-2-nitrobenzeneHCID 2311790297.4%

Reaction Steps

A solution of 4-(2-morpholinoethoxy)-3-nitrobenzaldehyde hydrochloride obtained in Step 1 (2.97 g, 9.38 mmol) in dichloromethane (10.0 mL) was added with trimethyl orthoformate (15.0 mL, 13.7 mmol) and a 10% solution of hydrogen chloride in methanol (5.00 mL), followed by stirring at room temperature for 4 hours. The reaction mixture was added with potassium carbonate (10.0 g, 72.4 mmol), then stirred at room temperature for 5 hours, and the solvent was evaporated under reduced pressure. The residue was added with water (50 mL) and was extracted with ethyl acetate (50 mL×3). After drying over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure to obtain 4-dimethoxymethyl-1-(2-morpholinoethoxy)-2-nitrobenzene (2.98 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919517B2
Source datasetuspto-grants-2011_04
ORD IDord-7a26484fe7ab416a8aaea2f238edf426
Source noteuspto-grants-2011_04