A facile synthesis of ω-aminoalkyl ammonium hydrogen phosphates
2012
Abstract A series of ω -aminoalkyl ammonium hydrogen phosphates were synthesized through a simple and efficient three-step method. The starting materials, ω -aminoalkyl alcohols (AC- n , with carbon number n = 3, 4, 5, 6), were amino-protected with 9-fluorenylmethyl chloroformate (Fmoc-Cl), followed by phosphorylation with POCl 3 and deprotection in piperidine/DMF. The structures of each intermediate and final product were confirmed by 1 H NMR, FTIR and mass spectrum. The yield of each step was about 77–92%, with a total yield higher than 56%. This new method was superior in low-cost raw materials, mild reaction temperatures (0–25 °C) and easy purification methods.
Keywords:
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
7
References
6
Citations
NaN
KQI