Реакция #2175445

Уравнение реакции

23-azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol

toluenesulfonyl chloride

pyridine

pyridine

→

3

Выход 25.0%

23-azido-3,6,9,12,15,18,21-heptaoxatricos-1-yl p-toluenesulfonate

Выход 25.0%

Условия реакции

Обработка

1. 1
   ДругоеThe solvent was evaporated
2. 2
   Другоеthe crude product was purified on SiO2 column
3. 3
   Другоеpurified on semipreparative HPLC (System E)

Методика

A solution of 23-azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol (800 mg, 2.02 mmol) in pyridine (4 mL) was added dropwise to the solution of toluenesulfonyl chloride (771 mg, 4.04 mmol) and 4-dimethylaminopyridine (100 mg) in pyridine (10 mL) at room temperature. The mixture was stirred for 24 hours at room temperature. The solvent was evaporated and the crude product was purified on SiO2 column using hexanes/ethylacetate gradient 0-100% followed by ethylacetate/methanol gradient 0-100%, then purified on semipreparative HPLC (System E) to yield 280 mg (25%) of 3 as a colorless oil. 1H NMR (400 MHz, CDCl3): δ 2.45 (s, 3H), 3.38 (t, J=5.02 Hz, 2H), 3.58-3.70 (m, 28H), 4.16 (t, J=5.00 Hz, 2H), 7.34 (d, J=8.4 Hz, 2H), 7.80 (d, J=8.4 Hz, 2H); 13C NMR (100.6 MHz, CDCl3): δ 21.6, 50.7, 68.7, 69.2, 70.0, 70.5-70.8, 128.0, 129.7, 133.1, 144.7; MS ESI (m/z): [M+H]+ calcd. for C23H39N3O10S 549.24; found 549.9.

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