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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hepta-1,6-dien-4-amine | HCID 12791689 | — |
| 反応物 | 4-Chlorobutyldimethyldodecylammonium bromide | HCID 15870133 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-(N,N-Dimethyl-N-dodecylammonio)butyldiallylmethylammonium Chloride Bromide | HCID 86593803 | 67.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06610283B1 |
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| 出典データセット | uspto-grants-2003_08 |
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| ORD ID | ord-ca68ff58234a4e23b8c52b21d7ba058e |
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| 出典メモ | uspto-grants-2003_08 |
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