HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487078Generated: November 1, 2026
Styrene-4-sulfonyl chloride → N-(4-ethylphenyl)-N-isobutyl-4-vinylbenzenesulfonamide
https://huagongshe.com/reaction/1487078
Participants
| Role | Name | HCID | Charge |
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| Reactant | Styrene-4-sulfonyl chloride | HCID 9855777 | — |
| Reactant | 4-ethyl-N-(2-methylpropyl)aniline | HCID 28479385 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(4-ethylphenyl)-N-isobutyl-4-vinylbenzenesulfonamide | HCID 89876082 | — |
Reaction Steps
To a solution of 4-ethyl-N-isobutylaniline (400 mg, 2.256 mmol) in pyridine (5 mL) stirred in air at room temperature was added 4-vinylbenzene-1-sulfonyl chloride (760 mg, 3.75 mmol) in one charge. The reaction mixture was stirred at 20° C. for 30 minutes then stood for 16 hours. The solvent was evaporated in vacuo (Vaportec V10) to give the crude product, which was then purified by silica (Si) chromatography (0-50% ethyl acetate-cyclohexane gradient). The appropriate fractions were combined and evaporated in vacuo to give the required product, 940 mg, as a colourless gum. LCMS [LCMS1] Rt 1.44 min, m/z (ES+) 344 (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-579fe86de9f74e41b83d567f1d5cab48 |
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| Source note | uspto-grants-2016_08 |
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