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

HRID 628490
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HRID 628490 반응식
[Cl-].[Cl-].[Cl-].[Al+3].[N-:5]=[N+:6]=[N-:7].[Na+].[F:9][CH:10]([F:22])[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14](N=C=O)[C:13]=1[CH3:21].N([O-])=O.[Na+].Cl.[CH3:28][N:29](C)[CH:30]=[O:31]>O>[CH3:21][C:13]1[C:12]([O:11][CH:10]([F:9])[F:22])=[CH:17][CH:16]=[CH:15][C:14]=1[N:5]1[C:30](=[O:31])[N:29]([CH3:28])[N:7]=[N:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 6

HCID 313Hydrochloric AcidHCID 6228DimethylformamideHCID 33557Sodium AzideHCID 6451240Aluminum(III) ChlorideHCID 23668193Sodium NitriteHCID 898758031-Difluoromethoxy-3-isocyanato-2-methylbenzene

생성물 1

HCID 89875900
1-(2-Methyl-3-difluoromethoxyphenyl)-4-methyl-1,4-dihydrotetrazol-5-one

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Under ice-cooling, to a mixture of N,N-dimethylformamide 200 ml and aluminium trichloride 5.91 g was added sodium azide 2.64 g, and the resulting mixture was stirred for one hour. Thereto was then added 1-difluoromethoxy-3-isocyanato-2-methylbenzene 7.36 g and the reaction mixture was heated to 75° C. and was stirred for nine hours. The reaction mixture was cooled and under ice-cooling to the reaction mixture was added ice water 50 ml, followed by an addition of a mixture of sodium nitrite 4.1 g and water 100 ml. The resulting mixture was acidified with concentrated hydrochloric acid to make it pH about 4. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated saline and then was dried over anhydrous magnesium sulfate and was then concentrated under reduced pressure. To the resulting residues containing 1-(2-methyl-3-difluoromethoxyphenyl)-1,4-dihydrotetrazole-5-one was added N,N-dimethylformamide 100 ml, potassium carbonate 7.66 g, dimethyl sulfate 9.32 g, and the resulting mixture was stirred at room temperature for four hours. Thereto was added water 100 ml, and the resulting mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated saline, and dried over anhydrous magnesium sulfate and was then concentrated under reduced pressure. The resulting residue was subjected to a silica gel column chromatography to give 1-(2-methyl-3-difluoromethoxyphenyl)-4-methyl-1,4-dihydrotetrazole-5-one 1.0 g.

후처리

  1. stirringwas stirred for nine hours
  2. temperatureThe reaction mixture was cooled and under ice-
  3. temperaturecooling to the reaction mixture
  4. extractionThe resulting mixture was extracted with ethyl acetate
  5. washThe organic layer was washed with water and saturated saline
  6. dry with materialwas dried over anhydrous magnesium sulfate
  7. concentrationwas then concentrated under reduced pressure
  8. additionTo the resulting residues containing 1-(2-methyl-3-difluoromethoxyphenyl)-1,4-dihydrotetrazole-5-one
  9. additionwas added N,N-dimethylformamide 100 ml, potassium carbonate 7.66 g, dimethyl sulfate 9.32 g
  10. stirringthe resulting mixture was stirred at room temperature for four hours
  11. additionThereto was added water 100 ml
  12. extractionthe resulting mixture was extracted with ethyl acetate
  13. washthe organic layer was washed with water and saturated saline
  14. dry with materialdried over anhydrous magnesium sulfate
  15. concentrationwas then concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-46b7cb60f38143a3a07cf1826e13f192
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09314023B2

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