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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045199Generated: October 26, 2026

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

https://huagongshe.com/reaction/1045199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant(Oxan-4-yl)methanolHCID 2773573—
Reactant3-Cyano-4-fluorobenzene-1-sulfonamideHCID 25139897—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-cyano-4-((tetrahydro-2H-pyran-4-yl)methoxy)benzenesulfonamideHCID 67126413—

Reaction Steps

To (tetrahydro-2H-pyran-4-yl)methanol (0.206 g) in tetrahydrofuran (5 mL) was added sodium hydride (0.284 g) and the reaction stirred at room temperature for 20 minutes. The reaction was cooled to 0° C. and 3-cyano-4-fluorobenzenesulfonamide (0.355 g) in tetrahydrofuran (2 mL) was added dropwise and the reaction was allowed to warm to room temperature. After 3 hours, the reaction was poured into water, made acidic (pH=1) with 1N HCl and extracted with dichloromethane (2×75 mL). The organics were combined, washed with brine (50 mL), dried over magnesium sulfate, filtered and concentrated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563735B2
Source datasetuspto-grants-2013_10
ORD IDord-49ab25b6ab8a4d98ba80bd02866bc14b
Source noteuspto-grants-2013_10