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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821437Generated: November 2, 2026

Water → [2-(4-Formyl-2-methoxy-3-nitrophenoxy)ethyl]propane-1-sulfonamide

https://huagongshe.com/reaction/1821437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-Propanesulfonyl chlorideHCID 66279—
Reactant2-(4-Dimethoxymethyl-2-methoxy-3-nitrophenoxy)ethylamineHCID 68999463—
SolventTetrahydrofuranHCID 8028—
Product[2-(4-Formyl-2-methoxy-3-nitrophenoxy)ethyl]propane-1-sulfonamideHCID 8662822462.6%

Reaction Steps

A solution of 2-(4-dimethoxymethyl-2-methoxy-3-nitrophenoxy)ethylamine (0.5 g, 1.8 mmol) obtained in Step 3 in THF (10 mL) was added with triethylamine (0.38 mL, 2.7 mmol) and n-propanesulfonyl chloride (0.24 mL, 2.2 mmol), followed by stirring at room temperature for 3 hours. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The residue was added with methanol (6.0 mL) and 1 mol/L hydrochloric acid, followed by stirring for 15 minutes. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure to obtain [2-(4-formyl-2-methoxy-3-nitrophenoxy)ethyl]propane-1-sulfonamide (0.39 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605272B2
Source datasetuspto-grants-2009_10
ORD IDord-aada1a53d84d4e73a5821c2af168b354
Source noteuspto-grants-2009_10