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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487052Generated: October 31, 2026

Sodium hydride → N-(2,4-dimethylphenyl)-N-isobutyl-4-((oxetan-3-ylmethoxy)methyl)benzenesulfonamide

https://huagongshe.com/reaction/1487052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantOxetan-3-ylmethanolHCID 11521066—
Reactant4-(bromomethyl)-N-(2,4-dimethylphenyl)-N-isobutylbenzenesulfonamideHCID 86731585—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductN-(2,4-dimethylphenyl)-N-isobutyl-4-((oxetan-3-ylmethoxy)methyl)benzenesulfonamideHCID 72190527—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of oxetan-3-ylmethanol (7 mg, 0.075 mmol) and 4-(bromomethyl)-N-(2,4-dimethylphenyl)-N-isobutylbenzenesulfonamide (31 mg, 0.075 mmol) in 2-methyltetrahydrofuran (2-MeTHF) (1 mL) stirred under nitrogen at room temperature was added sodium hydride (60% dispersed in oil, approximately 2 mg, 0.075 mmol). The reaction mixture was stirred at 20° C. for 3 hours then quenched with water (75 uL). The solvent was removed under a stream of nitrogen to give the crude product. The crude was then purified by mass directed autoprep (ammonium carbonate modifier). The appropriate fractions were concentrated under a stream of nitrogen to give the required product, 2.4 mg. LCMS [LCMS1] Rt 1.34 min, m/z (ES+) 418 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428452B2
Source datasetuspto-grants-2016_08
ORD IDord-766aeea53d47415395dc7f1c2c82b2c8
Source noteuspto-grants-2016_08