HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397226Generated: 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/397226
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-(3-Chloropropyl)-N,N-dimethyl-1-dodecanaminium bromide | HCID 10861601 | — |
| Reactant | Hepta-1,6-dien-4-amine | HCID 12791689 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(N,N-dimethyl-N-dodecylammonio) propyldiallylmethylammonium Chloride Bromide | HCID 86593801 | 73.4% |
Reaction Steps
A mixture of 22 g diallylmethylamine and 74 g 3-chloropropyldodecyldimethyl-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 dialilymethylamine 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06610283B1 |
|---|
| Source dataset | uspto-grants-2003_08 |
|---|
| ORD ID | ord-ade318e45a7f46f696deb49c509df514 |
|---|
| Source note | uspto-grants-2003_08 |
|---|