HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358425Generated: October 26, 2026
Potassium Carbonate → N-allyl-N-alpha-methylbenzyl-4-hydroxybenzenesulfonamide
https://huagongshe.com/reaction/358425
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzenesulfonyl chloride, 4-(benzoyloxy)- | HCID 190100 | — |
| Reactant | (1-Phenylethyl)(prop-2-EN-1-YL)amine | HCID 2793834 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-allyl-N-alpha-methylbenzyl-4-hydroxybenzenesulfonamide | HCID 187212 | 63% |
Reaction Steps
To a solution of 1.61 g (0.01 mol) of N-allyl-N-α-methylbenzylamine and 1.38 g of potassium carbonate in 15 ml of acetone was dropped a solution of 2.62 g (0.084 mol) of 4-benzoyloxybenzenesulfonyl chloride in 5 ml of acetone under ice-cooling conditions. The mixture was subjected to the reaction at room temperature for 30 minutes and then at 50° C. for 1 hour. After completion of the reaction, the inorganic salt was removed by filtration and the acetone was distilled off, then, the contents were admixed with 150 ml of a 20% potassium hydroxide solution in ethanol, followed by refluxing for 30 minutes. After completion of the reaction, the reaction mixture was poured into ice-water to permit crystals to precipitate. The crystals were washed with a dilute acidic solution and a dilute alkaline solution, followed by sufficiently washing with water, drying in vacuum and recrystallizing from a mixed solvent of benzene and n-hexane to obtain 2.00 g of N-allyl-N-α-methylbenzyl-4-hydroxybenzenesulfonamide (melting point 128° to 129° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04468245 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-b7cfe68a2627465f89365b0030191c4b |
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| Source note | uspto-grants-1984_08 |
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