Hydrochloric Acid → 1-(2-Methyl-3-chlorophenyl)-1,4-dihydrotetrazol-5-one

HRID 1048614ノート

反応式

HRID 1048614 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[N-:5]=[N+:6]=[N-:7].[Na+].[Cl:9][C:10]1[C:11]([CH3:19])=[C:12]([CH:16]=[CH:17][CH:18]=1)C(Cl)=O.[N:20]([O-])=O.[Na+].Cl.[O:25]1[CH2:29]CCC1>O>[CH3:19][C:11]1[C:10]([Cl:9])=[CH:18][CH:17]=[CH:16][C:12]=1[N:5]1[C:29](=[O:25])[NH:20][N:7]=[N:6]1

参加物

8

実験手順

A mixture of aluminium chloride 33.6 g, sodium azide 49.2 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-chloro-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 75.6 g and water 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-chlorophenyl)-1.4-dihydrotetrazole-5-one.

後処理

  1. temperaturewith heating
  2. temperatureunder reflux for two hours
  3. customAfter the reaction mixtures
  4. temperaturewere cooled under ice-
  5. temperaturecooling
  6. additionwas added
  7. stirringthe resulting mixtures were stirred
  8. temperaturewith heating
  9. temperatureunder reflux for ten hours
  10. temperatureAfter cooling the mixtures
  11. additionwas added
  12. customthe reaction mixtures
  13. stirringwith stirring
  14. extractionwere then extracted with ethyl acetate
  15. dry with materialThe organic layers were dried over anhydrous sodium sulfate
  16. concentrationwere then concentrated under reduced pressure

出典と根拠

ORDレコード
ord-0cbabd7d0a7f4b7983de1f60ec35d596
出典データセット
uspto-grants-2016_07
特許番号
US09380782B2

反応ノート

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