تفاعل #1135795
ord-403e7a438de74a10aec040243e727c0b
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةcooling
- 2أخرىTo the reaction mixtures
- 3درجة الحرارةcooling
- 4درجة الحرارةThe mixtures were raised to room temperature
- 5workup.STIRRINGwere stirred for fourteen hours
- 6أخرىTo the reaction mixtures
- 7استخلاصthe mixtures were extracted with ethyl acetate
- 8غسيلThe organic layers were washed with 10% hydrochloric acid, water and saturated saline
- 9تجفيفwere dried over anhydrous magnesium sulfate
- 10تركيزwere then concentrated under reduced pressure
الإجراء التجريبي
To a mixture of the above-mentioned 1-(2-methyl-3-chlorophenyl)-1,4-dihydrotetrazole-5-one 10.00 g and N,N-dimethylformamide 100 mL was added 55% sodium hydride 2.30 g under ice-cooling. The mixtures were raised to room temperature and were stirred for one hour. To the reaction mixtures was added methyl iodide 3.2 mL under ice-cooling. The mixtures were raised to room temperature and were stirred for fourteen hours. To the reaction mixtures was added water and the mixtures were extracted with ethyl acetate. The organic layers were washed with 10% hydrochloric acid, water and saturated saline, and were dried over anhydrous magnesium sulfate and were then concentrated under reduced pressure. The resulting residues were subjected to a silica gel column chromatography to give 1-(2-methyl-3-chlorophenyl)-4-methyl-1,4-dihydrotetrazole-5-one (hereinafter, referred to as “Intermediate (PRC-P)”) 1.56 g.