HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26391Generated: October 26, 2026
Aniline → N-benzene sulfonyl phenyl cyanamide
https://huagongshe.com/reaction/26391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Cyanogen Chloride | HCID 10477 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-benzene sulfonyl phenyl cyanamide | HCID 21323003 | 84.7% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04150051 |
|---|
| Source dataset | uspto-grants-1979_04 |
|---|
| ORD ID | ord-93251148a7124554a88961efd1b18c6f |
|---|
| Source note | uspto-grants-1979_04 |
|---|