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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26391Generated: October 26, 2026

Aniline → N-benzene sulfonyl phenyl cyanamide

https://huagongshe.com/reaction/26391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantDabcoHCID 9237—
ReactantCyanogen ChlorideHCID 10477—
SolventTetrahydrofuranHCID 8028—
ProductN-benzene sulfonyl phenyl cyanamideHCID 2132300384.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150051
Source datasetuspto-grants-1979_04
ORD IDord-93251148a7124554a88961efd1b18c6f
Source noteuspto-grants-1979_04