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Water → 3-(Azidomethyl)-5-(trifluoromethyl)isoxazole

HRID 1528379
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HRID 1528379 반응식
CS(O[CH2:6][C:7]1[CH:11]=[C:10]([C:12]([F:15])([F:14])[F:13])[O:9][N:8]=1)(=O)=O.[N-:16]=[N+:17]=[N-:18].[Na+].O>CN(C=O)C>[N:16]([CH2:6][C:7]1[CH:11]=[C:10]([C:12]([F:15])([F:14])[F:13])[O:9][N:8]=1)=[N+:17]=[N-:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 33557Sodium AzideHCID 86663141(5-(Trifluoromethyl)isoxazol-3-yl)methyl methanesulfonate

생성물 1

HCID 866631403-(Azidomethyl)-5-(trifluoromethyl)isoxazole수율 91.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 8.7 g (5-(trifluoromethyl)isoxazol-3-yl)methyl methanesulfonate in 87 mL DMF was added 9.23 g sodium azide. The reaction mixture was stirred 3 h at RT. 80 mL water was added under cooling. The mixture was extracted with diethyl ether (3×100 mL) and the organic layers were washed with water (3×100 mL) and then with sat. NaCl solution (1×100 mL). The combined organic layer was dried over Na2SO4, filtered off and concentrated in vacuo to yield 6.26 g of the title compound as a brown oil.

후처리

  1. temperatureunder cooling
  2. extractionThe mixture was extracted with diethyl ether (3×100 mL)
  3. washthe organic layers were washed with water (3×100 mL)
  4. dry with materialThe combined organic layer was dried over Na2SO4
  5. filtrationfiltered off
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-86dbfcb7266745fda41ec5452b570446
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09090599B2

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