Реакция #1135804

ord-bd4264cf8f3e40eba55e56cea9e49663

Уравнение реакции

O=N[O-].[Na+]
sodium nitrite
[Al+3].[Cl-].[Cl-].[Cl-]
aluminium chloride
[N-]=[N+]=[N-].[Na+]
sodium azide
C1CCOC1
tetrahydrofuran
Cc1c(I)cccc1C(=O)Cl
3-iodo-2-methylbenzoic acid chloride
C1CCOC1
tetrahydrofuran
Cl
hydrochloric acid
Cc1c(I)cccc1-n1nn[nH]c1=O
1-(2-methyl-3-iodophenyl)-1.4-dihydrotetrazole-5-one

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwith heating
  2. 2
    Температураunder reflux for two hours
  3. 3
    ДругоеAfter the reaction mixtures
  4. 4
    Температураwere cooled under ice-
  5. 5
    Температураcooling
  6. 6
    workup.ADDITIONwas added
  7. 7
    workup.STIRRINGthe resulting mixtures were stirred
  8. 8
    Температураwith heating
  9. 9
    Температураunder reflux for ten hours
  10. 10
    ТемператураAfter cooling the mixtures
  11. 11
    workup.ADDITIONwas added
  12. 12
    Другоеthe reaction mixtures
  13. 13
    workup.STIRRINGwith stirring
  14. 14
    Экстракцияwere then extracted with ethyl acetate
  15. 15
    СушкаThe organic layers were dried over anhydrous sodium sulfate
  16. 16
    Концентрированиеwere then concentrated under reduced pressure

Методика

A mixture of aluminium chloride 10.20 g, sodium azide 14.90 g and tetrahydrofuran 100 mL was stirred with heating under reflux for two hours. After the reaction mixtures were cooled under ice-cooling, and thereto was added a mixture of the above-mentioned 3-iodo-2-methylbenzoic acid chloride and tetrahydrofuran 100 mL and the resulting mixtures were stirred with heating under reflux for ten hours. After cooling the mixtures, to a mixture of sodium nitrite 22.90 g and water 200 mL was added the reaction mixtures with stirring. The mixtures were acidified with concentrated hydrochloric acid and were then extracted with ethyl acetate. The organic layers were dried over anhydrous sodium sulfate and were then concentrated under reduced pressure to give 1-(2-methyl-3-iodophenyl)-1.4-dihydrotetrazole-5-one.

Источник

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