HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1503084Erstellt: 25. Oktober 2026
2-Methoxyaniline → 4-methoxy-N-(2-methoxyphenyl)benzenesulfonamide
https://huagongshe.com/reaction/1503084
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Methoxyaniline | HCID 7000 | — |
| Edukt | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-methoxy-N-(2-methoxyphenyl)benzenesulfonamide | HCID 743417 | 75,3% |
Reaktionsschritte
To a solution of 4-methoxybenzenesulfonyl chloride (5.0 g, 24 mmol) and 2-methoxyaniline (3.0 g, 24 mmol) in dichloromethane (24 mL) at 0° C. was added triethylamine (3.4 mL, 24 mmol) over 10 minutes. The ice bath was removed, and the mixture was stirred for 16 hr. The mixture was diluted with dichloromethane (100 mL) and the combined solution was washed with water (50 mL) and brine (50 mL). The organic solution was dried over MgSO4, filtered, and evaporated, and the crude product was purified by silica gel chromatography (15-60% EtOAc/Hex). Product-containing fractions were pooled, evaporated, and dried under high vacuum to yield 5.3 g (44%) of the product as a tan-colored oil: 1H-NMR (CDCl3) δ 7.70-7.67 (d, 2H), 7.53-7.50 (d, 1H), 7.05-6.99 (m, 2H), 6.91-6.83 (m, 3H), 6.73 (d, 1H), 3.80 (s, 3H), 3.65 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09212134B2 |
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| Quelldatensatz | uspto-grants-2015_12 |
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| ORD ID | ord-27558dc9d9c345b6819f96b64c294c61 |
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| Quellennotiz | uspto-grants-2015_12 |
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