Реакция #706092

Уравнение реакции

cyclen

meso-2,5-dibromoadipic acid

lithium hydroxide

→

title product

Выход 51.8%

2,5-Bis-(1,4,7,10-tetraazacyclododecan-1-yl)hexan-1,6-dioic acid

Выход 51.8%

Растворители

water

Условия реакции

Обработка

1. 1
   ТемператураAfter cooling to ambient temperature
2. 2
   ПромывкаThe column was washed thoroughly with water (4 L)
3. 3
   Промывкаthe product was eluted with 0.5M acetic acid (2 L)
4. 4
   workup.ADDITIONFractions containing product

Методика

A mixture of cyclen (60.75 g, 350 mmol), meso-2,5-dibromoadipic acid (10.57 g, 35 mmol), and 1M lithium hydroxide (70 mL, 70 mmol) in water (104 mL) was heated to 60° C. under nitrogen for 170 hours. After cooling to ambient temperature, the reaction mixture was applied to an AG1X8 anion exchange column [400 mL (OH-form)]. The column was washed thoroughly with water (4 L), and the product was eluted with 0.5M acetic acid (2 L). Fractions containing product were combined, chased with water (3×200 mL) and ethanol (3×100 mL) to yield the title product (8.75 g, 51.8%) as a white, hygroscopic foam. Unreacted cyclen was reclaimed by concentration of the first 2 L of eluent and recrystallization from water. 1H NMR: (D2O) δ 2.75-2.90 (br mult, 34H), 1.52 (br, 4H). 13C NMR: (D2O) 24.3, 40.5, 41.1, 41.3, 41.6, 43.1, 44.9, 63.0, 177.1. MS (FAB): m/e 487.4 (MH+).

Источник