HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1599201Erstellt: 26. Oktober 2026
Sulfamic Acid → 4-(2-chloro-5-fluorosulphonylphenylazo)-N-ethyl-N-benzyl aniline
https://huagongshe.com/reaction/1599201
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sulfamic Acid | HCID 5987 | — |
| Edukt | N-Ethyl-N-benzylaniline | HCID 7098 | — |
| Edukt | Nitrosylsulfuric acid | HCID 82157 | — |
| Edukt | 3-Amino-4-chlorobenzenesulphonyl fluoride | HCID 97383 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Acetic propionic acid | HCID 131720610 | — |
| Produkt | 4-(2-chloro-5-fluorosulphonylphenylazo)-N-ethyl-N-benzyl aniline | HCID 53969731 | — |
Reaktionsschritte
3-Amino-4-chloro benzene sulphonyl fluoride (2 parts) was stirred in acetic/propionic acid 86/14 vol/vol (25 parts) and cooled to 0°-5° C. Nitrosyl sulphuric acid solution (3.8 parts) was added dropwise at 0°-5° C. and stirred under these conditions for 2 hours. The diazo solution was then added to a mixture of N-ethyl-N-benzyl aniline (2.7 parts), methanol (100 parts) and sulphamic acid (1 part) stirring at 0°-5° C. After stirring under these conditions for 30 mins, ice/water (100 parts) was added and the mixture stirred for a further 1 hour. The product was isolated by filtration, washed with water and pulled dry. The damp solid was then slurried in methanol (100 parts) and refiltered. Dried at 50° C. to yield 4-(2-chloro-5-fluorosulphonylphenylazo)-N-ethyl-N-benzyl aniline (2.3 parts).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05739299 |
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| Quelldatensatz | uspto-grants-1998_04 |
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| ORD ID | ord-559d64b2333f46a0803664a50d614084 |
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| Quellennotiz | uspto-grants-1998_04 |
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