HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086513Generated: October 29, 2026
Hepta-1,6-dien-4-amine → N-(N,N-Dimethyl-N-dodecylammonio)butyldiallylmethylammonium Chloride Bromide
https://huagongshe.com/reaction/2086513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hepta-1,6-dien-4-amine | HCID 12791689 | — |
| Reactant | 4-Chlorobutyldimethyldodecylammonium bromide | HCID 15870133 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(N,N-Dimethyl-N-dodecylammonio)butyldiallylmethylammonium Chloride Bromide | HCID 86593803 | 67.2% |
Reaction Steps
A mixture of 22 g of diallylmethylamine and 75 g 4-chlorobutyldimethyldodecylammonium bromide was dissolved in 100 mL of methanol and the reaction mixture was stirred at 65° C. for 48 hours. After cooling to room temperature, the solvent was removed under reduced pressure. The residual viscous oil was precipitated into 800 mL of ether with rapid stirring. The ether layer was decanted and the residue was again treated with 500 mL of 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06726905B1 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-4050f001cd5946a7a9dca2f132c2cc6a |
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| Source note | uspto-grants-2004_04 |
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