反応 #1135803

ord-3165a9601fae418282e1ca16d1af2c12

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度with heating
  2. 2
    温度under reflux for two hours
  3. 3
    その他After the reaction mixtures
  4. 4
    温度were cooled under ice-
  5. 5
    温度cooling
  6. 6
    workup.ADDITIONwas added
  7. 7
    workup.STIRRINGthe resulting mixtures were stirred
  8. 8
    温度with heating
  9. 9
    温度under reflux for ten hours
  10. 10
    温度After cooling the mixtures
  11. 11
    workup.ADDITIONwas added
  12. 12
    その他the reaction mixtures
  13. 13
    workup.STIRRINGwith stirring
  14. 14
    抽出were then extracted with ethyl acetate
  15. 15
    乾燥The organic layers were dried over anhydrous sodium sulfate
  16. 16
    濃縮were then concentrated under reduced pressure

実験手順

A mixture of aluminium chloride 181.0 g, sodium azide 265.0 g and tetrahydrofuran 30.0 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-bromo-2-methylbenzoic acid chloride and tetrahydrofuran 200 mL and the resulting mixtures were stirred with heating under reflux for ten hours. After cooling the mixtures, to a mixture of sodium nitrite 407 g and water 1,500 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-bromophenyl)-1.4-dihydrotetrazole-5-one.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09380782B2uspto-grants-2016_07