HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267707Generated: October 26, 2026
Aniline → N-benzene sulfonyl phenyl cyanamide
https://huagongshe.com/reaction/267707
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 | — |
Reaction Steps
To a 3 liter 3-necked flask equipped with a stirrer, addition funnel, thermometer, and drying tube was charged 93.1g (1.0 mole) of aniline, 111g (1.1 moles) of triethylene diamine and 250 ml. of tetrahydrofuran. To this reaction mixture was added dropwise a solution of 176.6g (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 111g of triethylene diamine and this solution was added dropwise to a solution of 87g (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 218g (84.7%) of N-benzene sulfonyl phenyl cyanamide, m.p. 65°-66°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03944526 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-a1f50fa75fff408784ff0ffdab73c51f |
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| Source note | uspto-grants-1976_03 |
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