HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 434217Erstellt: 23. Oktober 2026
Hydrochloric Acid → 4-Bromo-2-(4,5-dihydroisoxazol-3-yl)-3-methylbenzenesulfonyl chloride
https://huagongshe.com/de/reaction/434217
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sulfur Dioxide | HCID 1119 | — |
| Edukt | Benzenamine, 4-bromo-2-(4,5-dihydro-3-isoxazolyl)-3-methyl- | HCID 9813747 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Katalysator | Cupric Chloride | HCID 24014 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-Bromo-2-(4,5-dihydroisoxazol-3-yl)-3-methylbenzenesulfonyl chloride | HCID 18757253 | — |
Reaktionsschritte
At 15° C., a solution of 9 g (35 mmol) of 4-bromo-2-(4,5-dihydroisoxazol-3-yl)-3-methylaniline in 50 ml of glacial acetic acid is added to 15 ml of conc. hydrochloric acid. At 5-10° C., a solution of 2.44 g (35 mmol) of sodium nitrite in 10 ml of water is then added dropwise, and the mixture is stirred at 5° C. for 1 hour. At room temperature, this solution is then added dropwise to a mixture of a solution of 47 g (0.74 mol) of sulfur dioxide in 100 ml of glacial acetic acid and a solution of 2.23 g (13 mmol) of copper(II) chloride in 5 ml of water. The reaction mixture is stirred at room temperature for 1 hour and subsequently poured into 300 ml of ice-water and extracted with methylene chloride. The organic phase is washed with water, dried with magnesium sulfate and concentrated.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06670482B2 |
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| Quelldatensatz | uspto-grants-2003_12 |
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| ORD ID | ord-8ed6e712e2e047559628e9408efc6bc9 |
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| Quellennotiz | uspto-grants-2003_12 |
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