Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045185Generated: October 31, 2026

Water → 3-nitro-4-((tetrahydro-2H-pyran-4-yl)methoxy)benzenesulfonamide

https://huagongshe.com/reaction/1045185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant(Oxan-4-yl)methanolHCID 2773573—
Reactant4-Fluoro-3-nitrobenzenesulfonamideHCID 16782487—
SolventTetrahydrofuranHCID 8028—
Product3-nitro-4-((tetrahydro-2H-pyran-4-yl)methoxy)benzenesulfonamideHCID 67126458—

Reaction Steps

(Tetrahydro-2H-pyran-4-yl)methanol (2.0 g) in tetrahydrofuran (20 mL) was treated with 60% NaH (1.377 g). The mixture was stirred for 20 minutes at the room temperature. To this mixture was added 4-fluoro-3-nitrobenzenesulfonamide (2.84 g) portion-wise. The reaction was stirred for another 2 hours. The mixture was poured into water, neutralized with 10% HC1, and extracted with ethyl acetate three times. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was purified with flash column chromatography on silica gel eluting with 20%-60% ethyl acetate in hexanes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563735B2
Source datasetuspto-grants-2013_10
ORD IDord-e67350b1750c4fec817459210c08d1e0
Source noteuspto-grants-2013_10