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Thionyl Chloride → 3-[5-Chloro-1-(4-fluorophenyl)pentyl]pyridine

HRID 1638626
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반응식

HRID 1638626 반응식
S(Cl)([Cl:3])=O.[F:5][C:6]1[CH:11]=[CH:10][C:9]([CH:12]([C:18]2[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=2)[CH2:13][CH2:14][CH2:15][CH2:16]O)=[CH:8][CH:7]=1>>[Cl:3][CH2:16][CH2:15][CH2:14][CH2:13][CH:12]([C:18]1[CH:19]=[N:20][CH:21]=[CH:22][CH:23]=1)[C:9]1[CH:10]=[CH:11][C:6]([F:5])=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 14722561epsilon-(4-Fluorophenyl)-3-pyridinepentanol

생성물 1

HCID 147225623-[5-Chloro-1-(4-fluorophenyl)pentyl]pyridine수율 100%

실험 절차

64 Parts of thionyl chloride were added portionwise to 4 parts of ε-(4-fluorophenyl)-3-pyridinepentanol. Upon complete addition, stirring was continued for 2 hours at reflux temperature. The reaction mixture was evaporated and the residue was taken up in water. The whole was treated with sodium carbonate. The product was extracted twice with methylbenzene. The combined extracts were washed with water, dried, filtered and evaporated, yielding 3.7 parts (100%) of 3-[5-chloro-1-(4-fluorophenyl)pentyl]pyridine as a residue (int. 57).

후처리

  1. additionUpon complete addition
  2. temperatureat reflux temperature
  3. custom
The reaction mixture was evaporated
  • additionThe whole was treated with sodium carbonate
  • extractionThe product was extracted twice with methylbenzene
  • washThe combined extracts were washed with water
  • customdried
  • filtrationfiltered
  • customevaporated
  • 출처 및 근거

    ORD 기록
    ord-a7dcab7b379d43dda1cb7a67e40fc273
    출처 데이터셋
    uspto-grants-1989_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04880808

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