Diethyl Ether → 1-[1-(3,4-Dichlorophenyl)cyclopentyl]ethanone

HRID 266885노트

반응식

HRID 266885 반응식
C[Mg]I.[Cl:4][C:5]1[CH:6]=[C:7]([C:12]2(C#N)[CH2:16][CH2:15][CH2:14][CH2:13]2)[CH:8]=[CH:9][C:10]=1[Cl:11].CC[O:21][CH2:22][CH3:23]>>[Cl:4][C:5]1[CH:6]=[C:7]([C:12]2([C:22](=[O:21])[CH3:23])[CH2:16][CH2:15][CH2:14][CH2:13]2)[CH:8]=[CH:9][C:10]=1[Cl:11]

참가 물질

4

실험 절차

Methylmagnesium iodide (3M solution in ether; 100 ml) was added dropwise at 0° C. under nitrogen to a stirred solution of 1-(3,4-dichlorophenyl) cyclopentanecarbonitrile (48 g) in ether (100 ml), then the mixture was stirred at ambient temperature for 24 hours. The resulting solid was collected by filtration, washed with ether, and added in portions to an ice-cold mixture of water (200 ml) and concentrated hydrochloric acid (125 ml). The mixture was heated at 95° C. for 1 hour, then allowed to cool to ambient temperature. The product was extracted into ether (5×100 ml), and the combined extracts were washed with water (2×100 ml), dried over magnesium sulphate, and the solvent removed in vacuo. The residue was distilled to give 1-[1-(3,4-dichlorophenyl)cyclopentyl]ethanone as a pale yellow oil (31.9 g), b.p. 124°-128° C./0.5 mbar.

후처리

  1. filtrationThe resulting solid was collected by filtration
  2. washwashed with ether
  3. additionadded in portions to an ice-cold mixture of water (200 ml) and concentrated hydrochloric acid (125 ml)
  4. temperatureThe mixture was heated at 95° C. for 1 hour
  5. temperatureto cool to ambient temperature
  6. extractionThe product was extracted into ether (5×100 ml)
  7. washthe combined extracts were washed with water (2×100 ml)
  8. dry with materialdried over magnesium sulphate
  9. customthe solvent removed in vacuo
  10. distillationThe residue was distilled

출처 및 근거

ORD 기록
ord-0f35a9426e714904a682221b0f8c4343
출처 데이터셋
uspto-grants-1997_07
특허 번호
US05652271

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