Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573108Generated: October 25, 2026

Sodium hydride → 4-((1,4-Dioxan-2-yl)methoxy)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/573108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(1,4-Dioxan-2-yl)methanolHCID 12655091—
Reactant4-Fluoro-3-nitrobenzenesulfonamideHCID 16782487—
SolventTetrahydrofuranHCID 8028—
Product4-((1,4-Dioxan-2-yl)methoxy)-3-nitrobenzenesulfonamideHCID 67126477—

Reaction Steps

(1,4-Dioxan-2-yl)methanol (380 mg) in tetrahydrofuran (30 mL) was treated with sodium hydride (60%, 245 mg) at room temperature for 30 minutes. The reaction mixture was cooled in an ice bath and 4-fluoro-3-nitrobenzenesulfonamide (675 mg) was added. The resulting mixture was stirred at room temperature for 2 hours and another portion of sodium hydride (60%, 245 mg) was added. The reaction mixture was stirred overnight and quenched with ice water (3 mL). The cloudy mixture was filtered and the filtrate was concentrated. The residue was triturated with methanol to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029404B2
Source datasetuspto-grants-2015_05
ORD IDord-eea82168b3a0460aa372d1d97b12aa7f
Source noteuspto-grants-2015_05