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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Oxetan-3-ylmethanol | HCID 11521066 | — |
| Reactant | 4-(bromomethyl)-N-(2,4-dimethylphenyl)-N-isobutylbenzenesulfonamide | HCID 86731585 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Product | N-(2,4-dimethylphenyl)-N-isobutyl-4-((oxetan-3-ylmethoxy)methyl)benzenesulfonamide | HCID 72190527 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428452B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-766aeea53d47415395dc7f1c2c82b2c8 |
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| Source note | uspto-grants-2016_08 |
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