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HRID 397227作成日:2026年10月25日

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

https://huagongshe.com/reaction/397227

反応式

関与物質

役割名称HCID仕込み量
反応物Hepta-1,6-dien-4-amineHCID 12791689—
反応物4-Chlorobutyldimethyldodecylammonium bromideHCID 15870133—
溶媒MethanolHCID 887—
生成物N-(N,N-Dimethyl-N-dodecylammonio)butyldiallylmethylammonium Chloride BromideHCID 8659380367.2%

反応条件

温度65 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06610283B1
出典データセットuspto-grants-2003_08
ORD IDord-ca68ff58234a4e23b8c52b21d7ba058e
出典メモuspto-grants-2003_08