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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532522Generated: October 26, 2026

N-(3-Chloropropyl)-N,N-dimethyl-1-dodecanaminium bromide → N-(N,N-dimethyl-N-dodecylammonio) propyldiallylmethylammonium Chloride Bromide

https://huagongshe.com/reaction/1532522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Chloropropyl)-N,N-dimethyl-1-dodecanaminium bromideHCID 10861601—
ReactantHepta-1,6-dien-4-amineHCID 12791689—
SolventMethanolHCID 887—
ProductN-(N,N-dimethyl-N-dodecylammonio) propyldiallylmethylammonium Chloride BromideHCID 8659380173.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 22 g diallylmethylamine and 74 g 3-chloropropyldodecyldimethylammonium 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 dialllymethylamine 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 70 g of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06203785B1
Source datasetuspto-grants-2001_03
ORD IDord-4c6acf801def4382b6149557782ee592
Source noteuspto-grants-2001_03