反应详情

A mixture of 3.12 g of tetrazole, 26.2 g of potassium carbonate, and 10 g of 4,4'-dichlorobenzhydryl chloride from above in 150 ml of dimethylformamide was heated under a nitrogen atmosphere for 2.5 hours at 85°-90° C. and then overnight at 60°-65° C. The reaction mixture was poured into 1 liter of a saturated aqueous sodium chloride solution which was then extracted twice with 200 ml portions of ethyl acetate. The combined organic extracts were washed three times with a saturated sodium chloride solution, dried over magnesium sulfate, and evaporated to dryness to provide 12.1 g of the crude product as a pale yellow oil. The residue was purified by high pressure liquid chromatography. The primary product which was recovered was 1.1 g of the 2-tetrazole derivative as white crystals when recrystallized from methanol, m.p. 91°-92° C. Mass spectral analysis confirmed that the product had the correct molecular formula (M+ =305) and 13C and 1H NMR NOE experiments confirmed that the primary product was 2-[bis(4-chlorophenyl)methyl]-2H-tetrazole.

1. temperaturewas heated under a nitrogen atmosphere for 2.5 hours at 85°-90° C.
2. customovernight
3. customat 60°-65° C
4. extractionwas then extracted twice with 200 ml portions of ethyl acetate
5. washThe combined organic extracts were washed three times with a saturated sodium chloride solution
6. dry with materialdried over magnesium sulfate
7. customevaporated to dryness