HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378385Generated: October 26, 2026
Benzenesulfonamide → N-[2-(5-Methyl-2-furanyl)ethyl]benzenesulfonamide
https://huagongshe.com/reaction/2378385
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 131725182 | HCID 131725182 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[2-(5-Methyl-2-furanyl)ethyl]benzenesulfonamide | HCID 21875493 | 23% |
Reaction Steps
Benzenesulfonamide (157 mg, 1.00 mmol) was added to a 10% aqueous solution of sodium hydroxide (0.40 mL, 1.0 mmol). A solution of compound 24A (280 mg, 1.00 mmol) in acetone (1 mL) was then added. The reaction mixture was heated at 90° C. for 8 h then cooled to room temperature. Ice was added and the mixture was extracted with CH2Cl2. The combined organic layers were washed with water, dried and concentrated under reduced pressure. Purification by flash chromatography on silica gel, eluting with CH2Cl2 gave 60 mg (0.23 mmol, 23%) of compound 24B as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07470797B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-b120f10d535e4886bc6b99db94684d30 |
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| Source note | uspto-grants-2008_12 |
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