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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769131Generated: November 1, 2026

N-Methyl-N-(4-methoxybenzyl)-4-(2-(methoxycarbonyl)ethenyl)phenylsulfonamid → HCID 19957094, compound

https://huagongshe.com/reaction/1769131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-N-(4-methoxybenzyl)-4-(2-(methoxycarbonyl)ethenyl)phenylsulfonamidHCID 54424125—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 19957094HCID 1995709482.3%

Reaction Steps

To a suspension of the sulfonamide of Example 331 (c) (2.1 g, 4.54 mmol) in ethanol (125 mL) under nitrogen was added 10% Pd/C (0.6 g). The mixture was placed on a Parr hydrogenator at 50 psi of hydrogen for 2 hours, the catalyst was removed by filtration and the solvent was removed in vacuo. The residue was recrystallized from Et2O/MeOH, extracted with CH2Cl2, washed with water, then brine and was dried over MgSO4. The solvent was removed in vacuo to afford 1.41 g (82%) of N-methyl-N-(4-methoxybenzyl)-4-(2-(methoxycarbonyl)ethyl)phenylsulfonamide as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380721
Source datasetuspto-grants-1995_01
ORD IDord-a626c51d44af4965ae7dd5b3f2021a56
Source noteuspto-grants-1995_01