反应详情

A suspension of 1-H-tetrazole (2.0 g, 28.5 mmol) and potassium carbonate (5.9 g, 42.7 mmol) in DMF (30 mL) was treated with benzyl chloromethyl ether (5.36 g, 34.2 mmol), and the mixture was stirred for 4 hours. Analysis by LC/MS indicated that the reaction was not complete, so the reaction was treated with benzyl chloromethyl ether (0.5 g, 3.19 mmol) and stirred overnight. The mixture was filtered, and the filtrate was concentrated in-vacuo. The residue was diluted with diethyl ether (200 mL), washed 5× with water (50 mL), once with brine, dried over sodium sulfate, and concentrated in-vacuo. The residue was purified over a 6×20 mm silica gel column, eluting with 20% then 30% ethyl acetate/hexanes to yield the title compound (2.39 g, 44% yield), and 1-(benzyloxymethyl)-2H-tetrazole (2.56 g, 47% yield).

1. stirringstirred overnight
2. filtrationThe mixture was filtered
3. concentrationthe filtrate was concentrated in-vacuo
4. additionThe residue was diluted with diethyl ether (200 mL)
5. washwashed 5× with water (50 mL)
6. dry with materialonce with brine, dried over sodium sulfate
7. concentrationconcentrated in-vacuo
8. customThe residue was purified over a 6×20 mm silica gel column
9. washeluting with 20%