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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075436Generated: October 31, 2026

Hydrochloric Acid → 3-Methanesulfonylamino-4-(2-morpholinoethoxy)benzaldehyde

https://huagongshe.com/reaction/2075436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Dimethoxymethyl-2-(2-morpholinoethoxy)anilineHCID 23117901—
SolventDichloromethaneHCID 6344—
Product3-Methanesulfonylamino-4-(2-morpholinoethoxy)benzaldehydeHCID 2311789595%

Reaction Steps

A solution of 5-dimethoxymethyl-2-(2-morpholinoethoxy)aniline obtained in Step 3 (0.27 g, 0.91 mmol) in dichloromethane (2.00 mL) was added with methanesulfonyl chloride (0.11 mL, 1.42 mmol) and pyridine (0.50 mL, 6.18 mmol), followed by stirring at room temperature for 10 hours. The reaction mixture was added with hydrochloric acid (3 mol/L, 3.00 mL), was stirred at room temperature for 20 minutes, was neutralized with a saturated aqueous sodium hydrogencarbonate solution (50 ml) and was extracted with ethyl acetate (50 mL×3). The organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure. the crude product was purified by silica gel column chromatography (chloroform, then methanol/chloroform=1/6) to obtain 3-methanesulfonylamino-4-(2-morpholinoethoxy)benzaldehyde (0.28 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919517B2
Source datasetuspto-grants-2011_04
ORD IDord-10a1455f3c814ca6a634ba8e02987fd0
Source noteuspto-grants-2011_04