HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26391Erstellt: 25. Oktober 2026
Aniline → N-benzene sulfonyl phenyl cyanamide
https://huagongshe.com/reaction/26391
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Aniline | HCID 6115 | — |
| Edukt | Benzenesulfonyl chloride | HCID 7369 | — |
| Edukt | Dabco | HCID 9237 | — |
| Edukt | Cyanogen Chloride | HCID 10477 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-benzene sulfonyl phenyl cyanamide | HCID 21323003 | 84,7% |
Reaktionsschritte
To a 3 liter 3-necked flask equipped with a stirrer, addition funnel, thermometer, and drying tube was charged 93.1 g (1.0 mole) of aniline, 111 g (1.1 moles) of triethylene diamine and 250 ml. of tetrahydrofuran. To this reaction mixture was added dropwise a solution of 176.6 g (1 mole) of benzenesulfonyl chloride in 300 ml. of tetrahydrofuran. The reaction mixture was stirred at room temperature for 2.5 hours and was then filtered. To the filtrate was added 111 g of triethylene diamine and this solution was added dropwise to a solution of 87 g (1.41 moles) of cyanogen chloride in 100 ml. of THF which was maintained at -5° C. with cooling. After this addition was complete the stirred reaction mixture was allowed to return to room temperature over a 161/2 hour period. The reaction mixture was filtered and the filament was added to water to precipitate the product. The product was recrystallized from aqueous methanol to yield 218 g (84.7%) of N-benzene sulfonyl phenyl cyanamide, m.p. 65°-66° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04150051 |
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| Quelldatensatz | uspto-grants-1979_04 |
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| ORD ID | ord-93251148a7124554a88961efd1b18c6f |
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| Quellennotiz | uspto-grants-1979_04 |
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