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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706872Generated: October 25, 2026

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

https://huagongshe.com/reaction/706872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant(Oxan-4-yl)methanolHCID 2773573—
Reactant4-Fluoro-3-nitrobenzenesulfonamideHCID 16782487—
SolventWaterHCID 962—
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 solution was stirred for 20 minutes at the room temperature. To this solution 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% HCl, 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 numberUS09174982B2
Source datasetuspto-grants-2015_11
ORD IDord-4409d3be38a14b008ca3a4d5e3fed870
Source noteuspto-grants-2015_11