HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604575Generated: October 25, 2026
Water → N-(3-Oxo-3-phenylpropyl)methanesulfonamide
https://huagongshe.com/reaction/604575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloropropiophenone | HCID 70295 | — |
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(3-Oxo-3-phenylpropyl)methanesulfonamide | HCID 57423897 | 21.1% |
Reaction Steps
Methanesulfonamide (0.476 g, 5.00 mmol) was dissolved in N,N-dimethyl-formamide (DMF, 10 mL), and 60% sodium hydride (0.275 g, 5.00 mmol) was added at 0° C., then the mixture was stirred at the same temperature for 20 minutes. Subsequently, to the mixture was added 3-chloropropiophenone (843 mg, 5.00 mol), and the mixture was stirred at the same temperature for 2 hours, and then further stirred at room temperature for 15 hours. To the mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=20/1) to give N-methanesulfonyl-3-aminopropiophenone (240 mg, 21%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910611B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-0ca34d6cf74d4f5e8573cb62c8b8fd5d |
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| Source note | uspto-grants-2011_03 |
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