Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706883Generated: October 30, 2026

Water → 3-Chloro-4-(2-(2-methoxyethoxy)ethylthio)benzenesulfonamide

https://huagongshe.com/reaction/706883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant3-Chloro-4-fluorobenzenesulfonamideHCID 7509883—
Reactant2-(2-Methoxyethoxy)ethane-1-thiolHCID 11400802—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-4-(2-(2-methoxyethoxy)ethylthio)benzenesulfonamideHCID 67126664—

Reaction Conditions

Temperature110 °C

Reaction Steps

In a 25 mL microwave tube was added sodium hydride (0.6 g) in tetrahydrofuran (10 mL) to give a suspension. 2-(2-Methoxyethoxy)ethanethiol (1 g) was added slowly. After stirring for 30 minutes, 3-chloro-4-fluorobenzenesulfonamide (1.54 g) dissolved in 10 mL tetrahydrofuran was added slowly. The mixture was heated at 110° C. for 30 minutes in a Biotage Initiator microwave reactor. Water was added, the product was extracted with ether (20 mL×3), dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. The crude product was purified by flash chromatography on silica eluting with 0-25% ethyl acetate in hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174982B2
Source datasetuspto-grants-2015_11
ORD IDord-1123995efa294aa4ba04185bc9e0e5d7
Source noteuspto-grants-2015_11