HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272664Generated: October 26, 2026
Ammonia → 2,4-dimethyl-1,6-ditetradecylpyridinium Hexafluorophosphate
https://huagongshe.com/reaction/272664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tetradecylamine | HCID 16217 | — |
| Reactant | 2,4-Dimethyl-6-tetradecylpyrylium hexafluorophosphate | HCID 11539671 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,4-dimethyl-1,6-ditetradecylpyridinium Hexafluorophosphate | HCID 11520222 | 26% |
Reaction Steps
2,4-Dimethyl-6-tetradecylpyrylium hexafluorophosphate (10, n=13, 1.5 g, 3.33 mmol) was dissolved in 15 mL chloroform and treated with 0.71 g (3.33 mmol) of tetradecylamine (11, m=13). Triethylamine (0.5 mL) was then added to the brown-yellow solution, which was subsequently refluxed for 5 minutes, treated with 1 mL of acetic acid and refluxed for another hour. The homogenous mixture was treated with 0.2 mL of concentrated aqueous ammonia, refluxed for 5 min., cooled and extracted with 10 mL of water to solve the precipitated inorganic salts. After separation, the chloroform layer was dried on sodium sulfate and evaporated to dryness to yield 2.00 g of crude product. This product was purified by means of flash chromatography (Silica gel 60) using a 20/80 methanol/chloroform (v/v) mobile phase to yield 0.56 g (22%) of pure product, which was recrystallized from ethanol to yield 0.54 g of crystalline compound (12, m=n=13).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456197B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-522d95feea284699ba5b2bcab6c85853 |
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| Source note | uspto-grants-2008_11 |
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