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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640032Generated: October 27, 2026

Triethylamine → N-cyclohexyl-N'-hexadecylsulfamide

https://huagongshe.com/reaction/640032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHexadecylamineHCID 8926—
ReactantSodium CarbonateHCID 10340—
ReactantCyclohexylsulfamyl chlorideHCID 12914615—
SolventDichloromethaneHCID 6344—
ProductN-cyclohexyl-N'-hexadecylsulfamideHCID 6857900379%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 13.6 g of the cyclohexylsulfamoyl chloride (69 mmol) in 100 mL of dichloromethane is added under argon atmosphere to a solution of 1-hexadecylamine (19.9 g, 82 mmol) and triethylamine (47.5 mL, 340 mmol) in 300 mL of dichloromethane. The reaction mixture is stirred 5 hours at 0° C., neutralized with an aqueous Na2CO3 solution and concentrated under reduced pressure. The residue is taken up in dichloromethane (800 mL). The organic components are successively washed with diluted hydrochloric aqueous solution, NaHCO3 aqueous solution and brine, dried (Na2SO4), and concentrated under reduced pressure. The residue is suspended in ether, filtered through Büchner, and the precipitate is washed two times with 100 ml of ether to yield a white powder of N-cyclohexyl-N′-hexadecylsulfamide (21.8 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691929B2
Source datasetuspto-grants-2010_04
ORD IDord-2ce0015573b343abbf3d7d36d0f5e3e1
Source noteuspto-grants-2010_04