HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247965Generated: November 1, 2026
Iodoethane → N-(3-acetylphenyl)-N-ethyl-4-methylbenzenesulfonamide
https://huagongshe.com/reaction/1247965
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | N-(3-Acetylphenyl)-4-methylbenzenesulfonamide | HCID 220585 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(3-acetylphenyl)-N-ethyl-4-methylbenzenesulfonamide | HCID 20280466 | — |
Reaction Steps
A 29 g portion of N-(3-acetylphenyl)-4-methylbenzenesulfonamide was dissolved in 250 ml of dimethylformamide with stirring. This mixture was treated with 6.5 g of sodium methoxide and stirred for 30 minutes, then 20 g of ethyl iodide was added. This mixture was stirred at room temperature for one hour, then at reflux for 5 hours. The dimethylformamide was removed in vacuo, the residue shaken with 150 ml of water, the mixture adjusted to pH 4 with 10N sodium hydroxide and then cooled to 0° C. The precipitate was collected, washed twice with water and then air dried, giving 31.5 g of N-(3-acetylphenyl)-N-ethyl-4-methylbenzenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04521422 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-79a78215d79d4734b818b9fb08dcdda8 |
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| Source note | uspto-grants-1985_06 |
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