Water → HCID 67045723、化合物

HRID 1810606ノート

反応式

HRID 1810606 の反応式
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:19]=[CH:18][C:9]([C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:11])=[CH:8][CH:7]=1.[CH2:20]([NH2:24])[CH2:21][CH2:22]C.O.[OH-].[Na+].[C:28](#N)C>>[CH3:22][CH2:21][CH:20]([NH:24][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:19]=[CH:18][C:9]([C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:11])=[CH:8][CH:7]=1)[CH3:28]

参加物

6

反応物 5

HCID 962WaterHCID 6342AcetonitrileHCID 8007ButylamineHCID 14798Sodium HydroxideHCID 10934655HCID 10934655、化合物

生成物 1

HCID 67045723HCID 67045723、化合物

反応条件

温度
70 °C

実験手順

10 g (36 mmol) 4-(3-chloropropoxy)benzophenone was dissolved in 100 mL acetonitrile. 26.3 g (0.36 mol) n.-butyl amine was added and the mixture was heated to 70° C. for 30 hours. The solvent was evaporated under reduced pressure and the residue was treated with 500 mL water. The pH was adjusted to pH=1. The mixture was stirred for one hour at 40° C. The mixture was cooled to 10° C. and the precipitated compounds were isolated by filtration. The precipitate was treated with 200 mL water and the pH was adjusted to 12, using a 1 N NaOH-solution. The mixture was extracted with 200 mL methylene chloride. The organic fraction was dried over MgSO4 and evaporated under reduced pressure. The crude 4-[(3-butylamino)propoxy]benzophenone was purified by preparative column chromatography on a SVP D40 Merck-Np column, using a gradient elution from methylene chloride to methanol at a flow rate of 40 mL per minute. 4.4 g of 4-[(3-butylamino)propoxy]benzophenone was isolated.

後処理

  1. customThe solvent was evaporated under reduced pressure
  2. additionthe residue was treated with 500 mL water
  3. temperatureThe mixture was cooled to 10° C.
  4. customthe precipitated compounds were isolated by filtration
  5. extractionThe mixture was extracted with 200 mL methylene chloride
  6. dry with materialThe organic fraction was dried over MgSO4
  7. customevaporated under reduced pressure
  8. customThe crude 4-[(3-butylamino)propoxy]benzophenone was purified by preparative column chromatography on a SVP D40 Merck-Np column
  9. washa gradient elution from methylene chloride to methanol at a flow rate of 40 mL per minute

出典と根拠

ORDレコード
ord-0c833bb58ee6403bac36c898b0a50c8d
出典データセット
uspto-grants-2013_01
特許番号
US08362101B2

反応ノート

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