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3-Chloro-1-propanol → 3-[p-(3-Hydroxypropoxy)benzoyl]indole

HRID 247559
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HRID 247559 반응식
[OH:1][C:2]1[CH:18]=[CH:17][C:5]([C:6]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[NH:10][CH:9]=2)=[O:7])=[CH:4][CH:3]=1.Cl[CH2:20][CH2:21][CH2:22][OH:23]>CN(C)C=O.C[O-].[Na+]>[OH:23][CH2:22][CH2:21][CH2:20][O:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([C:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[NH:10][CH:9]=2)=[O:7])=[CH:17][CH:18]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 123133-Chloro-1-propanolHCID 30626713-(p-Hydroxy)benzoyl indole

생성물 1

HCID 136694983-[p-(3-Hydroxypropoxy)benzoyl]indole

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 10942334Sodium Methoxide용매

반응 조건

온도
110 °C

실험 절차

5 g of 3-(p-hydroxybenzoyl) indole were dissolved in 50 ml of dimethylformamide containing 2.28 g of sodium methoxide. 4.0 g of 3-chloropropanol was added to the solution followed by stirring at 110° C. in oil bath for 3 hours. After cooling, the solution was concentrated and extracted with 100 ml of ethyl acetate and 50 ml of water. The organic layer obtained was concentrated, and then the residue was purified by column chromatography on silica gel. Crude product was recrystallized from ethyl acetate to give 3-[p-(3-hydroxypropoxy)benzoyl]indole (compound 23) in the form of white needle crystals. (Yield: 30.5%).

후처리

  1. temperatureAfter cooling
  2. concentrationthe solution was concentrated
  3. extractionextracted with 100 ml of ethyl acetate and 50 ml of water
  4. customThe organic layer obtained
  5. concentrationwas concentrated
  6. customthe residue was purified by column chromatography on silica gel
  7. customCrude product was recrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-3a41a8799db94481aee317a672da15a7
출처 데이터셋
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04708961

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