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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789662Generated: November 1, 2026

Water → 4-[(2-methylsulfonyl-ethyl)-(4-fluoro-benzyl)-amino]-N-ethyl-benzenesulfonamide

https://huagongshe.com/reaction/1789662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-[(2-methylthio-ethyl)-(4-fluoro-benzyl)-amino]-N-ethyl-benzenesulfonamideHCID 22036215—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
Product4-[(2-methylsulfonyl-ethyl)-(4-fluoro-benzyl)-amino]-N-ethyl-benzenesulfonamideHCID 22036161100%

Reaction Steps

A solution of Oxone® (0.54 g, 0.88 mmol) in H2O (2 mL) was added to a 0° C. solution of 4-[(2-methylthio-ethyl)-(4-fluoro-benzyl)-amino]-N-ethyl-benzenesulfonamide (0.13 g, 0.34 mmol) in MeOH (8 mL) resulting in an immediate precipitate. After 1 h, the mixture was partitioned between CH2Cl2 and H2O. The aqueous layer was extracted with CH2Cl2 (2×). The combined organic layer was dried (Na2SO4), filtered, and evaporated in vacuo to afford 0.14 g (100%) of 4-[(2-methylsulfonyl-ethyl)-(4-fluoro-benzyl)-amino]-N-ethyl-benzenesulfonamide as a pale glass; (m+H)+ 415.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071177B2
Source datasetuspto-grants-2006_07
ORD IDord-cc91ba7f425e451d989228df5b9a3e76
Source noteuspto-grants-2006_07