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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629635Generated: October 29, 2026

Water → 4-(2-(2-Methoxyethoxy)ethylthio)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/629635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-(2-Methoxyethoxy)ethane-1-thiolHCID 11400802—
Reactant4-Fluoro-3-nitrobenzenesulfonamideHCID 16782487—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-(2-(2-Methoxyethoxy)ethylthio)-3-nitrobenzenesulfonamideHCID 67126460—

Reaction Steps

In a 100 mL round-bottomed flask 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 the mixture stirred for 30 minutes, 4-fluoro-3-nitrobenzenesulfonamide (1.616 g) in 10 ml tetrahydrofuran was added slowly. After the mixture stirred overnight, water was added slowly, and ethyl acetate (20 ml×3) was used to extract the product. The combined organic layers were dried over Na2SO4. After the mixture was filtered and concentrated, the crude product was added to a silica gel column and purified eluting with 0-10% methanol in dichloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315488B2
Source datasetuspto-grants-2016_04
ORD IDord-d5f95e944a0146cc910a700ada15e60d
Source noteuspto-grants-2016_04