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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272664생성일: 2026년 10월 26일

Ammonia → 2,4-dimethyl-1,6-ditetradecylpyridinium Hexafluorophosphate

https://huagongshe.com/reaction/272664

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물TriethylamineHCID 8471—
반응물TetradecylamineHCID 16217—
반응물2,4-Dimethyl-6-tetradecylpyrylium hexafluorophosphateHCID 11539671—
용매Acetic AcidHCID 176—
용매ChloroformHCID 6212—
생성물2,4-dimethyl-1,6-ditetradecylpyridinium HexafluorophosphateHCID 1152022226%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456197B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-522d95feea284699ba5b2bcab6c85853
출처 메모uspto-grants-2008_11