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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267707Generated: October 26, 2026

Aniline → N-benzene sulfonyl phenyl cyanamide

https://huagongshe.com/reaction/267707

Reaction equation

Participants

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03944526
Source datasetuspto-grants-1976_03
ORD IDord-a1f50fa75fff408784ff0ffdab73c51f
Source noteuspto-grants-1976_03