2-Indanone → HCID 58107514、化合物

HRID 1810205ノート

反応式

HRID 1810205 の反応式
CO[C:3](=O)[CH2:4][CH2:5][NH:6][CH2:7][CH3:8].[CH2:10]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:12][C:11]1=[O:19]>C1(C)C=CC=CC=1>[CH2:7]([N:6]1[C:11](=[O:19])[CH2:10][CH2:18][C:17]2[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:3]=3[CH2:4][C:5]1=2)[CH3:8]

参加物

4

反応物 2

HCID 119832-IndanoneHCID 76973Methyl N-ethyl-beta-alaninate

生成物 1

HCID 58107514HCID 58107514、化合物収率 27.1%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

3-Ethylamino-propionic acid methyl ester (2.41 g, 18.4 mmol) is added to a solution of 2-indanone (2.3 g, 17.33 mmol) in toluene (27 mL), and the reaction is brought to reflux for 2 hours. Toluene is removed in vacuo and the residue is dissolved in ethylene glycol (23 mL) and the resulting solution is heated to reflux for 8 hours. The reaction is allowed to cool to ambient temperature and is poured over water and extracted with dichloromethane. The organic phase is dried over magnesium sulfate and concentrated in vacuo to afford the crude title compound. The crude product is purified by silica gel chromatography (gradient of ethyl acetate in hexanes 10-100%) affording 1 g (27% yield) of the title compound. MS (m/z): 213.3 (M+1).

後処理

  1. temperatureto reflux for 2 hours
  2. customToluene is removed in vacuo
  3. dissolutionthe residue is dissolved in ethylene glycol (23 mL)
  4. temperaturethe resulting solution is heated
  5. temperatureto reflux for 8 hours
  6. additionis poured over water
  7. extractionextracted with dichloromethane
  8. dry with materialThe organic phase is dried over magnesium sulfate
  9. concentrationconcentrated in vacuo
  10. customto afford the crude title compound
  11. customThe crude product is purified by silica gel chromatography (gradient of ethyl acetate in hexanes 10-100%)

出典と根拠

ORDレコード
ord-a49627fa3f564e37980055b92400d622
出典データセット
uspto-grants-2013_01
特許番号
US08362063B2

反応ノート

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