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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397227Generated: October 26, 2026

Hepta-1,6-dien-4-amine → N-(N,N-Dimethyl-N-dodecylammonio)butyldiallylmethylammonium Chloride Bromide

https://huagongshe.com/reaction/397227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHepta-1,6-dien-4-amineHCID 12791689—
Reactant4-Chlorobutyldimethyldodecylammonium bromideHCID 15870133—
SolventMethanolHCID 887—
ProductN-(N,N-Dimethyl-N-dodecylammonio)butyldiallylmethylammonium Chloride BromideHCID 8659380367.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 22 g diallylmethylamine and 75 g 4-chlorobutyldimethyldodecyl-ammonium bromide were dissolved in 100 mL methanol and the reaction mixture was stirred at 65° C. for 48 hours. The progress of the reaction was monitored by the disappearance of the diallylmethylamine by thin layer chromatography (TLC). After cooling to room temperature, the solvent was removed under reduced pressure. The residual viscous oil was precipitated into 800 mL dry ether with rapid stirring. The ether layer was decanted and the residue was again treated with 500 mL dry ether. After stirring for 15 minutes the solvent was removed and the oily residue was dried under vacuum at 35° C. for 48 hours, yielding 65 g of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610283B1
Source datasetuspto-grants-2003_08
ORD IDord-ca68ff58234a4e23b8c52b21d7ba058e
Source noteuspto-grants-2003_08