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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532523Generated: October 26, 2026

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

https://huagongshe.com/reaction/1532523

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-chlorobutyldimethyldodecylammonium 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 numberUS06203785B1
Source datasetuspto-grants-2001_03
ORD IDord-9391c00cc64847a195d8f270f002dc2a
Source noteuspto-grants-2001_03