Реакция #1135801

ord-d442d0aec58746beb02aa3cf9068cbe7

Уравнение реакции

O=N[O-].[Na+]
sodium nitrite
Cl
hydrochloric acid
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
[N-]=[N+]=[N-].[Na+]
sodium azide
Cc1c(Br)cccc1N=C=O
1-bromo-3-isocyanato-2-methylbenzene
Cc1c(Br)cccc1-n1nn[nH]c1=O
1-(2-methyl-3-bromophenyl)-1,4-dihydrotetrazole-5-one
Выход 86.1%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe resulting mixtures were stirred for fifteen minutes
  2. 2
    ТемператураAfter cooling the mixtures
  3. 3
    workup.ADDITIONwas added the reaction solutions
  4. 4
    workup.STIRRINGwith stirring
  5. 5
    Экстракцияwere extracted with ethyl acetate
  6. 6
    ПромывкаThe organic layers were washed with water and saturated saline
  7. 7
    Сушкаwere dried over anhydrous magnesium sulfate
  8. 8
    Концентрированиеwere then concentrated under reduced pressure

Методика

Under ice-cooling, to N,N-dimethylformamide 220 mL was added anhydrous aluminum chloride 19.7 g and the resulting mixtures were stirred for fifteen minutes. Thereto was added sodium azide 9.6 g and the resulting mixtures were stirred for fifteen minutes and thereto was then added 1-bromo-3-isocyanato-2-methylbenzene 30.3 g and the resulting mixtures were heated at 80° C. for five hours. After cooling the mixtures, to a mixture of sodium nitrite 33 g, water 2 L and ice 500 g was added the reaction solutions with stirring. The mixtures were acidified with 10% hydrochloric acid and were extracted with ethyl acetate. The organic layers were washed with water and saturated saline, and were dried over anhydrous magnesium sulfate and were then concentrated under reduced pressure to give 1-(2-methyl-3-bromophenyl)-1,4-dihydrotetrazole-5-one 31.4 g.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09380782B2uspto-grants-2016_07