HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941011Generated: November 2, 2026
Sodium Hydroxide → Ammonium, (6-bromohexyl)trimethyl-, bromide
https://huagongshe.com/reaction/1941011
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 14625786 | HCID 14625786 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ammonium, (6-bromohexyl)trimethyl-, bromide | HCID 9857584 | — |
Reaction Steps
Six percent crosslinked poly(allylamine) was made as stated in Example 82. To a flask were added the crosslinked poly(allylamine) (12.5 grams; 6% crosslinked; ground to ~30 mesh), (3-bromopropyl)dodecyldimethylammonium bromide (17.5 grams; made by reaction of 1,3-dibromopropane and N,N-dimethyl-1-aminododecane in diethyl ether), and methanol (334 mL). The mixture was heated to 65° C. with stirring. Upon reaching 65° C., aqueous sodium hydroxide (1.14 grams of 50% solution) was added and the stirring continued at 65° C. for 2 hours. Two additional aliquots of aqueous sodium hydroxide (1.14 grams of 50% solution) were sequentially added and the stirring continued at 65° C. for an additional 2 hours for each aliquot. Aqueous sodium hydroxide (1.14 grams of 50% solution) was then added and the stirring continued at 65° C. for an additional 12 hours. The mixture was then allowed to cool to room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05702696 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-8a7d92446c7341d1818cb9fec649c4a9 |
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| Source note | uspto-grants-1997_12 |
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