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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591703Generated: November 1, 2026

N,N-Dimethylglycine → 4-(Methylsulfonylamino)benzaldehyde

https://huagongshe.com/reaction/591703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantMethanesulfonamideHCID 72879—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-(Methylsulfonylamino)benzaldehydeHCID 1892535558%

Reaction Steps

A mixture of 4-bromobenzaldehyde (0.250 g, 1.40 mmol), methanesulfonamide (0.154 g, 1.62 mmol), copper iodide (0.0510 g, 0.270 mmol), N,N-dimethylglycine (0.0280 g, 0.270 mmol), and potassium phosphate tribasic (0.716 g, 3.38 mmol) in DMF (5.00 mL) was stirred at reflux for 16 hours. The mixture was diluted with EtOAc (50 mL), washed with water (50 mL), and then saturated aqueous LiCl (5 mL). The combined aqueous layers were then back-extracted with EtOAc (50 mL). The organic layers were combined, washed with brine (50 mL), dried over Na2SO4, filtered, and the solvent was removed under reduced pressure, to provide N-(4-formylphenyl)methanesulfonamide (0.161 g, 58%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238640B2
Source datasetuspto-grants-2016_01
ORD IDord-744962b5dfe84183ae05aa2731c360d0
Source noteuspto-grants-2016_01