Ethyl Acetate → HCID 178424789, 화합물

HRID 1958859노트

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HRID 1958859 반응식
[CH3:1][C:2]1[CH:19]=[CH:18][CH:17]=[C:16]([CH3:20])[C:3]=1[CH2:4][O:5][C:6]1[C:7]([CH3:15])=[C:8]([CH2:12][C:13]#[N:14])[CH:9]=[CH:10][CH:11]=1.[N-:21]=[N+:22]=[N-:23].[Na+].[Cl-].[NH4+].C(OCC)(=O)C>CN(C=O)C.CCCCCC>[CH3:1][C:2]1[CH:19]=[CH:18][CH:17]=[C:16]([CH3:20])[C:3]=1[CH2:4][O:5][C:6]1[C:7]([CH3:15])=[C:8]([CH:9]=[CH:10][CH:11]=1)[CH2:12][C:13]1[NH:23][N:22]=[N:21][N:14]=1

참가 물질

7

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온도
90 °C

실험 절차

A mixture of 2-(3-(2,6-Dimethylbenzyloxy)-2-methylphenyl)acetonitrile (Step F, 2.70 g, 10.19 mmol), sodium azide (0.795 g, 12.23 mmol) and ammonium chloride (0.653 g, 12.22 mmol) in dry DMF (20 ml) was heated under argon at 90° C. for 16 hours or until all the starting material is consumed, the reaction mixture was cooled, diluted with water and extracted with EtOAc (30 ml×4). The combined organic layer was washed with brine, dried over Na2SO4, filtered, concentrated and purified by flash chromatography on a silica gel column (chloroform:methanol 92.5:7.5) to give semi solid product. The semi solid was stirred with 1:2 ethyl acetate:hexane (15 ml) for 10 minutes, and filtered to give product as a white solid.

후처리

  1. customis consumed
  2. temperaturethe reaction mixture was cooled
  3. additiondiluted with water
  4. extractionextracted with EtOAc (30 ml×4)
  5. washThe combined organic layer was washed with brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. custompurified by flash chromatography on a silica gel column (chloroform:methanol 92.5:7.5)
  10. customto give semi solid product
  11. filtrationfiltered
  12. customto give product as a white solid

출처 및 근거

ORD 기록
ord-271a7fe085d24c3bb35f1a2273bd4f1f
출처 데이터셋
uspto-grants-2013_04
특허 번호
US08410154B2

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