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

HRID 247559
ノート
印刷プレビュー

反応式

HRID 247559 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 10942334Sodium Methoxide溶媒

反応条件

温度
110 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-3a41a8799db94481aee317a672da15a7
出典データセット
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04708961

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート