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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTriethylamineHCID 8471—
ReactantTetradecylamineHCID 16217—
Reactant2,4-Dimethyl-6-tetradecylpyrylium hexafluorophosphateHCID 11539671—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
Product2,4-dimethyl-1,6-ditetradecylpyridinium HexafluorophosphateHCID 1152022226%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456197B2
Source datasetuspto-grants-2008_11
ORD IDord-522d95feea284699ba5b2bcab6c85853
Source noteuspto-grants-2008_11