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4-Toluenesulfonyl chloride → 3-(3,5-Difluorophenyl)propyl azide

HRID 247417
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HRID 247417 반응식
S(Cl)(C1C=CC(C)=CC=1)(=O)=O.[F:12][C:13]1[CH:14]=[C:15]([CH2:20][CH2:21][CH2:22]O)[CH:16]=[C:17]([F:19])[CH:18]=1.[N-:24]=[N+:25]=[N-:26].[Na+]>N1C=CC=CC=1.O>[F:12][C:13]1[CH:14]=[C:15]([CH2:20][CH2:21][CH2:22][N:24]=[N+:25]=[N-:26])[CH:16]=[C:17]([F:19])[CH:18]=1
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참가 물질

6

반응물 3

HCID 73974-Toluenesulfonyl chlorideHCID 33557Sodium AzideHCID 140499113-(3,5-Difluorophenyl)propan-1-ol

생성물 1

HCID 140499123-(3,5-Difluorophenyl)propyl azide수율 83.5%

시약·촉매·용매 2

HCID 962Water용매HCID 1049Pyridine용매

실험 절차

Tosyl chloride (0.0814 mol) was added to a cooled (0°) solution of 3-(3,5-difluorophenyl)propanol (0.0407 mol) in pyridine (75 ml). The reaction was stirred 2 hours at 25°, then it was poured into ice/water and extracted into ethyl ether. The ethereal extracts were washed with 3N aqueous hydrogen chloride and water, then were dried over sodium sulfate and concentrated. The residue was dissolved in dimethylformamide (75 ml) and sodium azide (0.0814 mol) was added. The reaction was stirred 8 hours, then was diluted with water and extracted into ethyl acetate. The organic extract was washed with 3N aqueous hydrogen chloride and water, then dried over sodium sulfate and concentrated to yield 6.7 g (64%) of an oily product.

후처리

  1. extractionextracted into ethyl ether
  2. washThe ethereal extracts were washed with 3N aqueous hydrogen chloride and water
  3. dry with materialwere dried over sodium sulfate
  4. concentrationconcentrated
  5. dissolutionThe residue was dissolved in dimethylformamide (75 ml)
  6. stirringThe reaction was stirred 8 hours
  7. extractionextracted into ethyl acetate
  8. extractionThe organic extract
  9. washwas washed with 3N aqueous hydrogen chloride and water
  10. dry with materialdried over sodium sulfate
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-26c53f7df3304878ab91ea1b84bfa8de
출처 데이터셋
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04707488

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